12 Medical Communication jobs in the United Kingdom

**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
**Medical Information Specialist with French**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
**Division Specific Information**
Within Medical Communications, we improve patient health by supplying medical information services to our customers, patients and healthcare providers. We engage with healthcare professionals, regulatory agencies and pharmaceutical customers to help them navigate regulatory and compliance requirements around the world. We run medical information inquiries, document adverse events and product complaints, report product launches, prepare standard responses to inquiries and develop process improvements for customer implementation.
**Discover Impactful Work:**
PPD is looking for medical information specialists for its growing Medical Communications department.
Start a career you will enjoy!
Join a team of energetic healthcare professionals supporting one or more pharmaceutical/biotech companies.
As a front-line specialist in our medical information contact center you will represent PPD and the client(s) by providing concise, accurate and non-promotional information regarding the client's medicinal products or devices to healthcare professionals and patients.
**A day in the Life:**
+ d client procedures
+ Receiving medical information enquiries through various communication channels and documenting them in the appropriate database
+ Triaging and responding to the medical enquiries using client approved resources
+ Identifying, capturing, reporting, and following up on adverse events and product complaints in compliance with established timelines and organizational, client and regulatory guidelines
+ Maintaining and demonstrating advanced knowledge of project and corporate policies and procedures
+ Attending team and client meetings
+ Performing assigned peer quality reviews
+ Performing other ad-hoc activities according to PPD
**Education**
+ A degree in a medical related field or life science degree e.g. Medicine, Pharmacy, Dentistry.
+ Fluency in French verbal and written.
+ Great communication skills in English
**Knowledge, Skills, Abilities**
+ Capability to efficiently use computer systems (hardware and software)
+ Organizational and time management skills
+ Attention to detail.
+ Customer service oriented - compassionate, empathetic, patient
+ Ability to work independently as well as part of a team
+ Ability to maintain a positive and professional manner in challenging circumstances.
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
Apply today! Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
**Accessibility/Disability** **Access**
Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include
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Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

**Use your scientific and foreign language expertise to join the** **world's leading comprehensive pharmaceutical safety services organization** **at on a fast-growing team performing medical information call center services. Apply your knowledge and expertise, including complex decision making, to review, assess and process safety and product quality information. Be a part of a global team to help ensure the safety profiles of products marketed around the world with development opportunities to ultimately provide oversight on projects and teams.**
**RESPONSIBILITIES**
**Provide phone support to health care professionals and consumers regarding adverse events, product quality complaints, medical inquiries, product support, and other needs as required. This does NOT include commercial sales support.**
**Receive, triage, review and process Lifecycle safety operational data. Perform data entry for tracking and Lifecycle safety databases, coding relevant medical terminology, writing descriptive narratives, generating queries pertinent to the case, performing quality control, assisting with reconciliation, driving case closure, coordinating translations.**
**Receive and document incoming telephone calls or emails from investigative sites or other sources reporting safety data.**
**Build a positive, collaborative team environment with Lifecycle safety team members, lead by example, provide training and mentoring for less experienced team members and operations staff.**
**Establish and maintain effective team project service operations communications**
**Liaise with Project Manager by proactively identifying issues and proposing solutions**
**Participate in training across Lifecycle safety process service offerings, participate in working groups as applicable in implementation of new initiatives**
**REQUIRED KNOWLEDGE, SKILLS AND ABILITIES**
**Must be a Pharmacist.**
**Excellent written and verbal skills in** **English (min. C1) and German language (min. C2 or native).**
**Willingness and aptitude to learn new skills across our Lifecycle Safety service lines.**
**Excellent attention to detail and accuracy maintaining consistently high-quality standards.**
**Excellent organizational skills and time management skills.**
**Ability to establish and maintain effective working relationships with coworkers, managers and clients.**
**Ability to work effectively on multiple projects simultaneously, organize own workload and effectively manage competing priorities.**
**MINIMUM REQUIRED EDUCATION AND EXPERIENCE**
**Bachelor's Degree in Pharmacy**
**Fluency in English (min. C1 level) and native level of German language.**
**This role is not available for UK visa sponsorship**
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at .
At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

**Use your scientific and foreign language expertise to join the** **world's leading comprehensive pharmaceutical safety services organization** **at on a fast-growing team performing medical information call center services. Apply your knowledge and expertise, including complex decision making, to review, assess and process safety and product quality information. Be a part of a global team to help ensure the safety profiles of products marketed around the world with development opportunities to ultimately provide oversight on projects and teams.**
**RESPONSIBILITIES**
**Provide phone support to health care professionals and consumers regarding adverse events, product quality complaints, medical inquiries, product support, and other needs as required. This does NOT include commercial sales support.**
**Receive, triage, review and process Lifecycle safety operational data. Perform data entry for tracking and Lifecycle safety databases, coding relevant medical terminology, writing descriptive narratives, generating queries pertinent to the case, performing quality control, assisting with reconciliation, driving case closure, coordinating translations.**
**Receive and document incoming telephone calls or emails from investigative sites or other sources reporting safety data.**
**Build a positive, collaborative team environment with Lifecycle safety team members, lead by example, provide training and mentoring for less experienced team members and operations staff.**
**Establish and maintain effective team project service operations communications**
**Liaise with Project Manager by proactively identifying issues and proposing solutions**
**Participate in training across Lifecycle safety process service offerings, participate in working groups as applicable in implementation of new initiatives**
**REQUIRED KNOWLEDGE, SKILLS AND ABILITIES**
**Must be a Pharmacist.**
**Excellent written and verbal skills in** **English (min. C1) and German language (min. C2 or native).**
**Willingness and aptitude to learn new skills across our Lifecycle Safety service lines.**
**Excellent attention to detail and accuracy maintaining consistently high-quality standards.**
**Excellent organizational skills and time management skills.**
**Ability to establish and maintain effective working relationships with coworkers, managers and clients.**
**Ability to work effectively on multiple projects simultaneously, organize own workload and effectively manage competing priorities.**
**MINIMUM REQUIRED EDUCATION AND EXPERIENCE**
**Bachelor's Degree in Pharmacy**
**Fluency in English (min. C1 level) and native level of German language.**
**This role is not available for UK visa sponsorship**
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at .
At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

**Use your scientific and foreign language expertise to join the** **world's leading comprehensive pharmaceutical safety services organization** **at on a fast-growing team performing medical information call center services. Apply your knowledge and expertise, including complex decision making, to review, assess and process safety and product quality information. Be a part of a global team to help ensure the safety profiles of products marketed around the world with development opportunities to ultimately provide oversight on projects and teams.**
**RESPONSIBILITIES**
**Provide phone support to health care professionals and consumers regarding adverse events, product quality complaints, medical inquiries, product support, and other needs as required. This does NOT include commercial sales support.**
**Receive, triage, review and process Lifecycle safety operational data. Perform data entry for tracking and Lifecycle safety databases, coding relevant medical terminology, writing descriptive narratives, generating queries pertinent to the case, performing quality control, assisting with reconciliation, driving case closure, coordinating translations.**
**Receive and document incoming telephone calls or emails from investigative sites or other sources reporting safety data.**
**Build a positive, collaborative team environment with Lifecycle safety team members, lead by example, provide training and mentoring for less experienced team members and operations staff.**
**Establish and maintain effective team project service operations communications**
**Liaise with Project Manager by proactively identifying issues and proposing solutions**
**Participate in training across Lifecycle safety process service offerings, participate in working groups as applicable in implementation of new initiatives**
**REQUIRED KNOWLEDGE, SKILLS AND ABILITIES**
**Must be a Pharmacist.**
**Excellent written and verbal skills in** **English (min. C1) and German language (min. C2 or native).**
**Willingness and aptitude to learn new skills across our Lifecycle Safety service lines.**
**Excellent attention to detail and accuracy maintaining consistently high-quality standards.**
**Excellent organizational skills and time management skills.**
**Ability to establish and maintain effective working relationships with coworkers, managers and clients.**
**Ability to work effectively on multiple projects simultaneously, organize own workload and effectively manage competing priorities.**
**MINIMUM REQUIRED EDUCATION AND EXPERIENCE**
**Bachelor's Degree in Pharmacy**
**Fluency in English (min. C1 level) and native level of German language.**
**This role is not available for UK visa sponsorship**
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at .
At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

Director, Global Medical Affairs Neuropsychiatry
Date: Jul 29, 2025
Location:
Harlow, United Kingdom, CM20 2FB
Company: Teva Pharmaceuticals
Job Id: 62688
**Who We Are**
Together, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It's a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world's leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization's Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we're always looking for new ways to continue making a difference, and new people to make a difference with.
**The Opportunity**
This is an exciting opportunity for an experienced medical affairs leader to shape the future of psychiatry at a global level. As Director of Global Medical Affairs, Neuropsychiatry, you will play a pivotal role in driving the medical and scientific strategy for psychiatry, working in close partnership with the Therapeutic Area (TA) lead and the wider GMANeuropsychiatryteam. You'll lead the development and execution of strategic plans to support the successful launch and lifecycle management of key assets, while building strong collaborations with external experts, scientific bodies, and patient representatives. This role offers the chance to provide influential medical guidance across early and late-stage development, as well as commercialised products, ensuring robust scientific leadership across clinical research, medical launch preparation, and health economics strategy.
Location:
Ideally, the successful candidate would be based within a commutable distance from either our Harlow or Ridings Points sites. However, we'd be open to receiving applications from those based anywhere across The UK, subject to your openness to national/international travel c.10%-20% of your working hours
**How You'll Spend Your Day**
**Key Responsibilities**
+ Medical and scientific leadership and support to current and future commercialized medicines, and issues management for current medicines within psychiatry
+ Responsible for the development and execution of the Global Medical Affairs plan for the relevant asset(s). These will include, amongst others, responsibilities such as Phase IV trial activities (such as protocol development, study execution, medical governance and interpretation of results); development of Key Opinion Leader (External Experts) strategy and plan; scientific congress activities (such as medical symposium, presentation of abstracts and or posters); input to publication strategy and review of Investigator Sponsored Studies/Collaborative Research/GHEVO studies.
+ In partnership with the TA lead and team provides coordination and execution of overall medical strategy for Teva's assets in psychiatry in close collaboration with Regional Medical Affairs teams, from initiation of regional pre-launch activities to several years post-launch (as relevant)
+ Again, alongside the TA lead contributes to and implements the world-wide medical psychiatry strategy
+ Interfaces effectively with other Global Medical Affairs functions such as Scientific Communications and Global Health Economics, Value and Outcomes, and other departments, including Commercial, Clinical Development, Regulatory Affairs and Pharmacovigilance
+ Provides counsel to clinical development with input on early and late-stage development plans, target product profile, and lifecycle management
+ Collaborates with Global Scientific Communications in support of knowledge generation for the psychiatry franchise, including strategy development and review of manuscripts, abstracts and posters as part of the publication team
+ Develops and maintains professional relationships with external experts and professional associations including therapeutic guideline development groups. Responsible for the External Expert interface for the respective psychiatry medicines
**Your Experience And Qualifications**
**Do you have.**
+ Preferably, a life sciences degree / MD / MPharm, PhD and at least five years pharmaceutical industry experience.
+ Experience in designing and executing PIV studies- this would be beneficial
+ Pharmaceutical industry experience in global medical affairs, ideally in psychiatry or neuroscience.
+ Experience in successfully developing strategy and executing medical plans, and in building professional external expert networks.
+ A broad knowledge of drug development, clinical trial design, regulatory requirements, business development and life cycle management.
**Are you.**
+ Able to build strong work relationships with all stakeholders involved
+ Able to work in a changing and flexible environment
+ Experienced and adept at working collaboratively across different cross-functional teams such as commercial, R&D, health outcomes, regulatory, pharmacovigilance and compliance.
+ Bringing a leadership skillset and comfort working within a matrix set-up
+ Able to translate complex scientific content into what this means in medical practice for the HCP and patient
+ Driven by the pride in your work
+ A strategic thinker
If so, we'd value hearing from you.
**Enjoy A More Rewarding Choice**
We support our people through every stage of their journey with us. Our flexible reward platform puts you in control, empowering you to tailor your benefits to fit your lifestyle, priorities, and what matters most to you. With 25 days of annual leave that grows with your service, the flexibility to purchase additional days, and two dedicated volunteering days each year, your time off is truly yours to enjoy, recharge, and give back. We prioritise your health with private medical insurance, life assurance, critical illness cover, and income protection.
Whether you're growing your family or pursuing new adventures, our enhanced maternity and paternity leave, sabbaticals, and hybrid working policies are here to support you through life's most meaningful moments. Financial wellbeing matters too, which is why we offer an enhanced pension scheme, access to a discount store, and free financial coaching through Bippit.
To help you grow with confidence, we offer a structured training and development programme tailored to your role and department, equipping you with the tools, knowledge, and support you need to thrive.
**Already Working @TEVA?**
#TJ If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site ( internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.
Application deadline for internal candidates will close on Tuesday 12th August 2025
**Teva's Equal Employment Opportunity Commitment**
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.
EOE including disability/veteran

**Job Description Summary**
The Medical Affairs Manager (MAM) plays a vital role in bridging scientific knowledge with strategic business objectives, acting as a non-promotional expert liaison between the organization and the external medical community. By leveraging deep clinical and diagnostic expertise-particularly in the pre-analytical phase-the MAM supports the commercial organization with scientific insights, educational initiatives, and evidence-based guidance. Core responsibilities include engaging with healthcare professionals, facilitating peer-to-peer scientific exchange, developing educational programs, supporting clinical research initiatives, and serving as a key resource in therapeutic and diagnostic areas. The MAM also contributes to the review of promotional materials, delivers strategic insights, and ensures the alignment of Medical Affairs objectives with internal and external stakeholder needs.
Success in this role requires a blend of scientific acumen, business understanding, and strong interpersonal skills. The ideal candidate will have expertise in laboratory medicine, clinical study design, and data interpretation, along with a solid grasp of industry regulations and diagnostic workflows. They must demonstrate strong project management skills, the ability to translate complex scientific information for diverse audiences, and a proven track record of relationship-building with key opinion leaders. Effective communication, adaptability, and a collaborative mindset are essential, as the MAM operates in a dynamic matrix environment, supporting both medical and commercial teams while maintaining a customer-centric approach.
**Job Description**
**We are the makers of possible**
BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.
**Why join us?**
A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time.
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow and thrive. And find satisfaction in doing your part to make the world a better place.
**Become a maker of possible with us!**
**About the role**
The Medical Affairs Manager (MAM) serves as a key local (Country/Hub) representative within the Medical Affairs team, acting as a strategic liaison between the organisation and external stakeholders. This role provides non-promotional product and scientific support to the commercial organisation by leveraging deep clinical knowledge, academic credentials, and scientific expertise in the relevant therapeutic and diagnostic areas.
The MAM engages with healthcare professionals, academic researchers, and scientific organisations to facilitate meaningful scientific exchange. These interactions ensure that key opinion leaders and institutions have access to accurate, up-to-date scientific information, while also enabling the organisation to gather and communicate valuable external insights to internal cross-functional teams.
A strong understanding of disease states, diagnostic pathways, emerging clinical evidence, and ongoing research-particularly in the pre-analytical phase-is essential. The MAM also contributes to the development and execution of the clinical research strategy, ensuring the safety and integrity of clinical studies involving licensed products and solutions.
**Main responsibilities will include:**
+ **Drive Strategic Initiatives** : Implement scientific and educational initiatives aligned with Medical Affairs goals.
+ Collaborate with Key Opinion Leaders and healthcare collaborators to establish and cultivate relationships.
+ **Scientific Expertise** : Serve as the primary clinical and scientific resource for HCPs in relevant therapeutic areas.
+ Education & Training: Develop and deliver programs to improve disease understanding and patient care.
+ **Customer Interaction** : Engage various audiences through meetings, group discussions, and symposium presentations.
+ **Advisory & Congress Support** : Facilitate expert involvement in advisory boards, meetings, and attend medical congresses to report insights.
+ **Material Review** : Act as Medical Reviewer/Approver for promotional content as assigned.
+ **Clinical Research Support** : Assist with Investigator Sponsored Studies and identify clinical trial sites and investigators.
+ **Cross-Functional Collaboration** : Support commercial initiatives while maintaining a primarily medical focus.
+ **Insight Delivery** : Provide strategic insights and competitive intelligence to guide internal decision-making.
**About you**
+ Strong flexibility and understanding of business operations.
+ In-depth understanding of methodologies, practice, and/or laboratory medicine, with particular expertise in the preanalytical phase of diagnostic workflows.
+ Solid knowledge of study design, data interpretation, and study evaluation.
+ Knowledge of regulations, standards, and industry guidelines.
+ Ability to manage, synthesise, and analyse data effectively.
+ Proven ability to build and maintain relationships with KOLs and the broader scientific/medical community.
+ Competency in clinical study design, statistical analysis, and technical/scientific writing.
+ Strong ability to interpret and communicate complex clinical and scientific information.
+ Excellent verbal, written, and presentation communication skills.
+ Demonstrated customer-centric approach and responsiveness.
+ Strong project management skills and ability to work effectively in a matrix environment.
**Click on apply if this sounds like you!**
At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting.
Becton, Dickinson and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics.
**To learn more about BD visit:** ** Skills
Optional Skills
.
**Primary Work Location**
GBR Winnersh - Eskdale Road
**Additional Locations**
DNK Herlev - Lyskær, SWE Stockholm - Marieviksgatan
**Work Shift**
At BD, we are strongly committed to investing in our associates-their well-being and development, and in providing rewards and recognition opportunities that promote a performance-based culture. We demonstrate this commitment by offering a valuable, competitive package of compensation and benefits programs which you can learn more about on our Careers Site under Our Commitment to You ( .
Salary or hourly rate ranges have been implemented to reward associates fairly and competitively, as well as to support recognition of associates' progress, ranging from entry level to experts in their field, and talent mobility. There are many factors, such as location, that contribute to the range displayed.
The salary or hourly rate offered to a successful candidate is determined by their experience, education, and skills, as well as the labor laws and Collective Bargaining Agreement (CBA) requirements applicable to the work location.
**Salary Range Information**
£57,400.00 - £97,600.00 GBP Annual
Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

For further inquiries regarding the following opportunity, please contact one of our Talent Specialist:
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Meghna at   br>
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Title: Medical Writing Consultant or Regulatory Affairs Medical Writer - Remote (Part Time) < r>
Location: Remote
Duration: 7 Months br>
Estimated Hours per Week : 20



Job Description:

As a Pharmaceutical Consultant, you will play a crucial role in providing medical writing direction and guidance for various projects. Your expertise will ensure that all documentation aligns with client's style guide and meets the necessary regulatory standards (US and EMA). You will be responsible for the following:

Key Responsibilities:

• Provide medical writing direction and guidance aligned with client's style guide for assigned projects, including the review of work products. < r>
• Convert relevant data and information into formats that comply with TM document requirements and coordinate the review of the final products. < r>
• Understand, assimilate, and interpret various sources of information with appropriate guidance and direction from the TM team. < r>
• Confirm the completeness and accuracy of information presented in documents. < r>
• Perform literature searches as needed to gather relevant content for drafting documents. < r>
• Maintain expert knowledge of US and international regulations, requirements, and guidance associated with scientific publications, including US FDA and ICH guidelines. < r>
• Utilize prior knowledge of preclinical strategy, pharmacology, toxicology, and GLP practices to ensure that documents drafted at client are prepared for regulatory inspection or audit in the US or Europe. < r>
• Complete draft reports based on data provided by client Subject Matter Experts (SMEs) to ensure thoroughness and compliance. < r>
• Review draft training modules on GLP’s, regulatory writing and FDA interactions and provide suggestions on ways to modernize.
Qualifications:

• Advanced degree in Life Sciences, Pharmacy, or a related field. < r>
• Proven experience in medical writing within the pharmaceutical or biotech industry. < r>
• Regulatory Affairs Certification and/or PMP certification < r>
• Strong understanding of regulatory requirements and guidance related to scientific publications. < r>
• Excellent analytical skills and attention to detail. < r>
• Ability to work collaboratively with cross-functional teams and communicate effectively. < r>
• Proficient in conducting literature searches and synthesizing information. < r>
• Excellent knowledge of English language < r>
• Attention to detail

**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At Thermo Fisher Scientific, you will discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner, and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development, and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
Summarized Purpose:
We are excited to be expanding our Medical Writing FSP Team in Europe. We are looking for a Principal Medical Writer to be dedicated to a client in the FSP space; experience in leading submissions would be preferred. We are seeking an experienced and highly skilled Regulatory Medical Writer to join our team. The role is be responsible for creating, reviewing, and managing a wide range of clinical and regulatory documents. This role requires a strong understanding of scientific concepts, exceptional writing skills, and the ability to communicate complex information clearly and concisely.
Key Responsibilities:
· Lead the development, writing, and editing of complex clinical and regulatory documents, including clinical study reports, protocols, investigator brochures, and regulatory submissions (e.g., INDs, NDAs, MAAs).
· Collaborate with cross-functional teams, including clinical development, regulatory affairs, biostatistics, and medical affairs, to ensure the accurate and timely completion of documents.
· Ensure documents align with regulatory guidelines, company standards, and industry best practices.
· Provide strategic input and guidance on document content, structure, and presentation.
· Mentor and provide oversight to junior medical writers and ensure high-quality deliverables.
· Manage multiple writing projects simultaneously and prioritize tasks effectively.
· Stay current with industry trends, guidelines, and regulatory requirements.
Education and Experience:
· Bachelor's degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification required; Advanced degree preferred.
· Regulatory writing experience that provides the knowledge, skills, and abilities to perform the role (comparable to 8+ years).
· Experience working in the pharmaceutical/CRO industry required.
· Experience in managing and directing complex medical writing projects required.
· EU CTR experience preferred.
· Experience working on structured content management system and AI-driven content creation, and familiarity with Natural Language Generation preferred.
Knowledge, Skills, and Abilities:
· Excellent organizational and program management skills
· Proven leadership skills to manage and mentor a team of medical writers.
· Extensive knowledge of regulatory guidelines and drug development processes
· Strong interpersonal and communication skills to build and maintain effective working relationships with colleagues and stakeholders
· Understanding of quality control processes to ensure compliance with regulatory requirements and internal standards
· Self-motivated and adaptable
· Excellent judgment; high degree of independence in decision making and problem solving
· Capable of mentoring and leading junior level staff
What We Offer:
At PPD clinical research services we hire the best, develop ourselves and each other, and recognize the power of being one team. We understand that you will want to grow both professionally and personally throughout your career, and therefore at PPD clinical research services you will benefit from an award-winning learning and development programme, ensuring you reach your potential?
As well as being rewarded a competitive salary, we have an extensive benefits package based around the health and well-being of our employees. We have a flexible working culture, where PPD clinical research services truly value a work-life balance. We have grown sustainably year on year but continue to offer a collaborative environment, with teams of colleagues eager to share expertise and have fun together. We are a global organization but with a local feel?
Our Mission is to enable our customers to make the world healthier, cleaner, and safer. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation, and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation, and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.