588 Medical Science Liaisons jobs in the United Kingdom

Pharmaceutical Science Industrial Placement 2026 - 2027 (RSSL, Reading)

Reading, South East Mondelez International

Posted 6 days ago

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**Job Description**
**Reading Scientific Services Ltd (RSSL)** is at the forefront of scientific analysis, research, consultancy and training. We provide services to the food, pharmaceutical and consumer goods industries and the parent company Mondelez International. RSSL's goal is to be a world class supplier of scientific services by offering scientific excellence coupled with industry leading customer service.
**Are You Ready to Make an Impact at RSSL?**
**Join Our Mission to Transform Lives Through Science, Innovation and Collaboration**
At Reading Scientific Services Ltd (RSSL), we lead the way in scientific analysis, research, consultancy, and training. We provide services to the food, pharmaceutical, and consumer goods industries, as well as our parent company, **Mondelez International** .
RSSL is dedicated to delivering world-class scientific solutions and outstanding customer service. Recognised for our excellence, we were awarded CRO of the Year at the 2023 OBN Awards, adding to our previous accolades Employer of the Year, Enlightened Employer and Women in Business.
**If you are passionate about driving innovation and making a real impact, RSSL is the place for you!**
Our industrial placements are 13 months long and during this time we'll make you an integral part of the team. We hope to help you expand your horizons and encourage both your personal and professional development.
**Life at RSSL**
As an **Pharmaceutical Science** placement student at RSSL, you will be responsible and accountable for your projects from start to finish. We have multiple opportunities available across our state-of-the-art laboratories, where each has their own specialisms.
For our Pharmaceutical Science placements, we will consider the following degrees - Chemistry (and related degrees such as Analytical Chemistry, Applied Chemistry, Medicinal Chemistry, Forensic Chemistry and Pharmaceutical Chemistry), Chemical Engineering, Biochemistry, Biological Sciences, Natural Sciences, Physics and Materials Science.
We are looking for students to join our Pharmaceutical Wet Chemistry and Speciality Pharmaceutical teams. Both teams perform a wide range of routine and specialised analyses for a variety of pharmaceutical and healthcare companies. As a placement student, you will be an integral part of the team and learn to work to GMP standards in our compliant laboratories. You will undertake a comprehensive training programme to perform routine testing of pharmaceutical raw materials, active pharmaceutical ingredients (API's), excipients and finished drug products against pharmacopoeia and client methods. The Wet Chemistry team perform techniques such as FTIR, UV-VIS Spectrophotometry, Specific Optical Rotation, Specific Gravity, Refractive Index and Osmolality. Whilst the Speciality Pharmaceutical team are more chromatography focused, using techniques including HPLC, IC, GC, AAS, ICP-OES, ICP-MS.
During the placement, you will be expected to plan and execute experiments related to your projects, produce technical reports/presentations, and periodically communicate your key findings to stakeholders. You will also have the opportunity to interact with other departments within RSSL and may also be expected to support other ongoing project activities outside of your immediate team. Where a project is required to be completed as art of your university degree, we will ensure to work with you and your supervisor to find a project which meets the requirements.
**Please be aware that this role may require handling of materials that may contain chemicals, solvents and allergens, and the appropriate protective wear will be supplied.**
**Candidate Requirements:**
Studying towards a suitable **scientific degree (detailed above)**
+ **2:1 degree predicted end grade** (or equivalent)
+ Self-motivated and driven
+ Naturally inquisitive and passionate about technical excellence
+ Can work with a level of autonomy, as well as within a team
+ Demonstrate strong analytical, communication and presentation abilities
+ Pro-active and ready to take on new responsibilities
+ Able to build strong relationships
+ Good working knowledge of MS Office
+ Able to travel (if required)
In return for your commitment, drive and enthusiasm, we offer an attractive benefits package within a highly successful international business that offers a competitive salary, 35 days annual leave (including bank holidays), contributory pension, life assurance, and a flexible benefits programme.
This position does not meet the minimum salary requirements for Skilled Worker visa sponsorship. Therefore, we are unable to consider applicants who require sponsorship. Applicants must already have the right to work in the UK.
We review applications on a first come, first served basis and reserve the right to close our vacancies early - therefore we recommend that you complete and submit your application as soon as possible.  
The assessment center will take place on the 3rd of December 2025 at our Reading site.
RSSL and Mondelēz are a diverse and inclusive employer with an objective to ensure a fair and equal hiring process. If you require any reasonable adjustments to apply or throughout our assessment process, please contact ** ** stating " **RSSL Pharmaceutical Science Industrial Placement** " as the subject.  
Our candidate requirements are based on criteria to enable you to succeed in the role. If you have narrowly missed the above requirements and there are extenuating circumstances that you would like us to consider, you can let us know by contacting ** ** stating " **RSSL Pharmaceutical Science Industrial Placement** " as the subject and attaching a letter to confirm your extenuating circumstances.
Website channel Unit Summary**
Reading Scientific Services Ltd (RSSL) is a cutting-edge contract research organisation (CRO), providing research, analysis and consultancy to the food, consumer goods and life science sectors. Whether we are creating new products, validating medicines or solving investigations, we take pride in being a leader in our field, serving clients from across 70 countries. Enriched by our parent company, Mondelēz International, our team are committed to transforming lives through science, innovation and collaboration.
**Curious about us and want to learn more?**
**Please explore** : Website ( YouTube LinkedIn ( Glassdoor
RSSL is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, colour, religion, gender, sexual orientation or preference, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law.
#RSSL
**Job Type**
Intern (Fixed Term)
Interns
Early Careers
At Mondelēz International, our purpose is to empower people to snack right through offering the right snack, for the right moment, made the right way. That means delivering a broader range of delicious, high-quality snacks that nourish life's moments, made with sustainable ingredients and packaging that consumers can feel good about.
We have a rich portfolio of strong brands - both global and local. Including many household names such as Oreo, belVita and LU biscuits; Cadbury Dairy Milk, Milka and Toblerone chocolate; Sour Patch Kids candy and Trident gum. We are proud to hold the number 1 position globally in biscuits, chocolate and candy as well as the No. 2 position in gum
Our 80,000 Makers and Bakers are located in our operations in more than 80 countries and are working to sell our products in over 150 countries around the world. They are energized for growth and critical to us living our purpose and values. We are a diverse community that can make things happen, and happen fast.
Join us and Make It An Opportunity!
Mondelez Global LLC is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected Veteran status, sexual orientation, gender identity, gender expression, genetic information, or any other characteristic protected by law. Applicants who require accommodation to participate in the job application process may contact for assistance.
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Medical Science Liaison (Pharmaceutical)

BS1 4RB Bristol, South West £70000 annum + bon WhatJobs

Posted 8 days ago

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full-time
Our client is a leading pharmaceutical company seeking a highly motivated and experienced Medical Science Liaison (MSL) to join their dynamic team. This crucial role serves as the primary scientific and medical communication link between the company and key opinion leaders (KOLs) in the medical and scientific community. The MSL will engage in peer-to-peer scientific exchange, present complex clinical data, and gather insights to support the company's research and development initiatives. This is a hybrid role, requiring travel to meet with KOLs and attend medical conferences, balanced with remote work for administrative tasks and planning.

You will build and maintain strong relationships with healthcare professionals, researchers, and investigators, serving as a trusted scientific resource. Responsibilities include responding to unsolicited requests for medical information, presenting clinical trial data, educating healthcare providers on the company's products, and providing feedback on disease state management and unmet medical needs. A deep understanding of the pharmaceutical industry, clinical research, and relevant therapeutic areas is essential. Excellent communication, presentation, and interpersonal skills are paramount for success in this externally facing role. The ability to synthesize complex scientific information and communicate it effectively to diverse audiences is key.

Key Responsibilities:
  • Establish and cultivate strong, peer-to-peer relationships with key opinion leaders (KOLs) and healthcare professionals (HCPs) in relevant therapeutic areas.
  • Serve as a primary scientific and medical resource for internal and external stakeholders.
  • Deliver scientific and clinical presentations on the company's products and research findings.
  • Respond accurately and efficiently to unsolicited requests for medical information.
  • Gather insights from KOLs and HCPs regarding disease state, treatment landscape, and unmet medical needs.
  • Support clinical trial activities, including investigator identification and trial site support.
  • Attend and participate in relevant medical congresses and scientific meetings.
  • Provide feedback to internal teams on market insights, competitive intelligence, and scientific trends.
  • Ensure compliance with all industry regulations, ethical guidelines, and company policies.
  • Contribute to the development of scientific and medical communication strategies.

Qualifications and Skills:
  • Advanced scientific degree (Pharm.D., Ph.D., M.D., or equivalent) in a relevant life science or healthcare field.
  • Significant experience as an MSL or in a similar medical affairs role within the pharmaceutical industry.
  • Deep understanding of a specific therapeutic area (e.g., Oncology, Cardiology, Neurology).
  • Exceptional scientific acumen and the ability to critically evaluate clinical data.
  • Outstanding communication, presentation, and interpersonal skills.
  • Proven ability to build and maintain strong professional relationships.
  • Strong understanding of regulatory and compliance guidelines within the pharmaceutical industry.
  • Ability to travel extensively and work independently.
  • Proficiency in data analysis and interpretation.
  • A strategic mindset and a proactive approach to problem-solving.
This hybrid role requires travel and offers a flexible working arrangement. If you are a highly knowledgeable and relationship-driven scientific professional, we encourage you to apply. The position is based in Bristol, South West England, UK .
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Lead Medical Science Liaison (Pharmaceutical)

ST4 7QF Staffordshire, West Midlands £75000 annum + bon WhatJobs

Posted 20 days ago

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full-time
Our client, a globally recognized pharmaceutical company, is looking for an experienced Lead Medical Science Liaison (MSL) to cover the Stoke-on-Trent and surrounding regions. This role operates on a hybrid model, requiring travel to key opinion leaders (KOLs) and stakeholders in the territory, with dedicated time for remote planning, reporting, and virtual engagement. The Lead MSL will serve as a crucial scientific and medical expert for a specific therapeutic area, building strong relationships with healthcare professionals and providing balanced, scientific information regarding our client's innovative medicines. You will be responsible for understanding the clinical practice and unmet medical needs within your territory, relaying this valuable insight back to the organization to inform strategy and development.

Key responsibilities include:
  • Developing and executing a territory-specific medical affairs plan in alignment with brand strategy.
  • Establishing and maintaining strong, credible relationships with KOLs, researchers, and other healthcare providers.
  • Presenting complex scientific data and clinical information on products in a clear and accurate manner.
  • Responding to unsolicited scientific inquiries from healthcare professionals.
  • Gathering and reporting insights on clinical practice, treatment trends, and competitive intelligence.
  • Supporting clinical trial activities, including investigator identification and study conduct.
  • Collaborating effectively with internal teams, including sales, marketing, clinical development, and regulatory affairs.
  • Delivering scientific training and education to internal and external stakeholders.
  • Attending and presenting at key medical congresses and symposia.

Qualifications:
  • Advanced scientific degree (Pharm.D., Ph.D., M.D.) in a relevant field.
  • Minimum of 5 years of experience as an MSL or in a similar medical affairs role within the pharmaceutical industry.
  • Proven therapeutic area expertise (specify relevant area if known).
  • Demonstrated ability to build strong relationships with KOLs and navigate complex stakeholder landscapes.
  • Excellent presentation, communication, and interpersonal skills.
  • Strong understanding of clinical research methodology and data interpretation.
  • Ability to work independently and manage a remote territory effectively.
  • Willingness to travel extensively within the assigned territory.

This is a fantastic opportunity for a seasoned MSL to take a leadership role, influence medical practice, and contribute to advancing patient care in the Stoke-on-Trent area through a flexible hybrid working arrangement.
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Clinical Research Associate/ Senior Clinical Research Associate

Barrington James

Posted today

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About the Company

A fast-growing, tech-enabled CRO and global site network that started life within a major biopharma before becoming fully independent. They’ve built a proprietary AI platform now used to run smarter, faster clinical trials — and are expanding rapidly with their own hospitals and trial sites in India, and plans for Brazil, Australia, and China.


Now ~50 people, they’re closing Series A and moving into a Series B raise with a major bio-capital investor already signed. 0

It’s a genuine startup culture — everyone contributes, collaborates, and grows together. They also offer stock options from CRA level up – showing they invest in their people.


As their first UK CRA hire , you’ll have a key role in their European growth. You’ll monitor sites across the UK and EU (Spain, Greece, Italy, France, Germany) , support feasibility/start-up, and help shape the company’s operational foundations.


You’ll thrive here if you:

  • Enjoy working autonomously in a small, fast-moving CRO.
  • Want to help build something, not just follow a process.
  • Can balance hands-on site work with cross-functional input.


What You’ll Need:

  • 3 - 5 years CRA experience (CRO or sponsor)
  • 5 - 7 years for a Senior CRA
  • Proven EU monitoring exposure
  • Solid knowledge of ICH-GCP & EU regs
  • UK base with willingness to travel
  • Startup or small-CRO experience is a big plus
  • Oncology Based Experience


What’s on Offer:

  • Competitive salary with higher flexibility for Senior CRA's
  • Fast-track growth in a scaling, global business
  • Exposure to AI-driven clinical operations
  • Collaborative culture with true ownership and visibility
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Clinical Research Physician

Preston, North West Planet Pharma

Posted today

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Job Description

Planet Pharma are partnered with a leading clinical research organisation, who are seeking an experienced Research Physician with a strong clinical background and the ability to make independent decisions in a research environment.


Requirements:

  • Minimum of 4 years’ experience in the NHS at Registrar level, including independent decision-making on the ward and running outpatient clinics.
  • Background in General Medicine / Acute Internal Medicine.
  • MRCP qualification.
  • GMC registered – candidates must provide their GMC number.
  • Right to work in the UK.
  • Experience or exposure to clinical trials would be highly advantageous.


Candidates must be proactive, clinically competent, and ready to contribute to high-quality research delivery.


If this role isn’t suitable for you, please let us know if you can refer anyone – any recommendations are much appreciated! Planet Pharma offers a competitive referral scheme so you will be rewarded for your help!


About Planet Pharma


Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.


Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognized by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.


We are an equal opportunities Recruitment Business and Agency.

We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.

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Clinical Research Coordinator

Torpoint, South West IQVIA

Posted today

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Join IQVIA as a Clinical Research Coordinator!


Are you passionate about clinical research and ready to make a real impact? Do you want to be part of a global leader in healthcare innovation? If so, we’d love to hear from you!


IQVIA is seeking a dedicated Clinical Research Coordinator to join our team in Torpoint , working 24 hours per week on a one year contract . This is a fantastic opportunity to contribute to cutting-edge clinical trials at a single site, supporting investigators and ensuring smooth study operations.


What You’ll Be Doing:

As a key member of the site team, you’ll play a vital role in supporting clinical research activities. Your responsibilities will include:

  • Supporting clinical studies in line with health and safety policies under the guidance of the Principal Investigator.
  • Maintaining study documentation including protocols, CRFs, and EDC systems.
  • Coordinating logistics for study schedules.
  • Assisting with data entry, quality checks, and resolving queries to ensure accuracy.
  • Supporting patient recruitment and eligibility screening.


What We’re Looking For:

We’re seeking someone who is proactive, detail-oriented, and passionate about clinical research. Ideally, you’ll bring:

  • At least 2 years’ experience as a Clinical Research Coordinator, Research Nurse, or Site Research Assistant.
  • Solid understanding of clinical trials and study-specific procedures.
  • Basic knowledge of medical terminology.
  • Strong IT skills, including MS Office (Access, Outlook, Excel, Word).
  • Excellent interpersonal and communication skills.
  • Strong organisational abilities and attention to detail.


Why IQVIA?

At IQVIA, you’ll be part of a collaborative and forward-thinking team that’s shaping the future of healthcare. We offer a supportive environment, meaningful work, and the chance to grow your career in clinical research.

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Clinical Research Physician

Wythenshawe, North West Medicines Evaluation Unit Ltd, an IQVIA business

Posted today

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Job Description

Exciting roles in cutting edge research, working with some of the most distinguished pharma companies in the UK and internationally

We’re offering

A rewarding career pathway for GMC registered physicians to become involved in the development of tomorrow’s medicines, in MHRA Phase I Accredited Unit with an international reputation.

The role

You will support a diverse range of clinical studies/trials involving patients and healthy volunteers, undertaking drug development programmes in a variety of therapeutic fields, including respiratory, dermatology, cardiovascular, endocrinology, and inflammatory disorders.


Key responsibilities

To provide medical care and oversight of clinical trial participants.


To fulfil role of sub investigator/ Principal investigator when delegated ensuring compliance with regulatory and ethical standards.


A critical role in the design, execution and oversight of clinical trials.


To provide support to clinical staff and all other department in study set up and execution of clinical trials.


Working under the supervision of Professor Dave Singh, Medical Director. Applicants must have completed foundation year programme training or equivalent.


MEU will offer you.

·   Competitive salary (dependant on experience)

·   Continuous professional development

·   29 days annual leave increasing to 33 after 5 years' service

·   Company pension scheme

·   Generous annual bonus

·   Healthcare plan

·   Free parking

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Clinical Research Coordinator

Nottingham, East Midlands Actalent

Posted today

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Job Description

This is an exciting opportunity with candidates to start and interview as soon as possible!


The Clinical Research Coordinator must have minimum 1 year clinical research experience as they need an individual who can work independently as well as part of a team. Day to day responsibilities will involve data entry, query resolution and admin.


Bonus to have:

Experience with Oncology

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Clinical Research Physician

York, Yorkshire and the Humber Planet Pharma

Posted today

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Job Description

Planet Pharma are partnered with a leading clinical research organisation, who are seeking an experienced Research Physician with a strong clinical background and the ability to make independent decisions in a research environment.


Requirements:

  • Minimum of 4 years’ experience in the NHS at Registrar level, including independent decision-making on the ward and running outpatient clinics.
  • Background in General Medicine / Acute Internal Medicine.
  • MRCP qualification.
  • GMC registered – candidates must provide their GMC number.
  • Right to work in the UK.
  • Experience or exposure to clinical trials would be highly advantageous.


Candidates must be proactive, clinically competent, and ready to contribute to high-quality research delivery.


If this role isn’t suitable for you, please let us know if you can refer anyone – any recommendations are much appreciated! Planet Pharma offers a competitive referral scheme so you will be rewarded for your help!


About Planet Pharma


Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.


Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognized by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.


We are an equal opportunities Recruitment Business and Agency.

We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.

This advertiser has chosen not to accept applicants from your region.

Clinical Research Physician

MAC Clinical Research

Posted today

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Job Description

We are seeking to appoint a CRP1 (Clinical Research Physician – level 1) to join our dedicated team at our clinic in Teesside. The focus of this role is to fulfil the role of Sub-Investigator and Principal Investigator (where delegated) in clinical research studies in compliance with the protocol and ICH/GCP.

We welcome applications from newly qualified doctors with 2 years of experience (FY 1&2 included) and no prior experience in clinical research. This is an ideal opportunity for candidates exploring an alternative to NHS or private sector.

If you have prior experience in research or you have a real interest in changing to a career in clinical research and bring additional years of experience, particularly in psychiatry, then we would like to hear from you too

Starting salary: £50,000

(additional considerations will be made for those that match some/all of the "desirable" criteria outlined in Key Skills)

KEY SKILLS, KNOWLEDGE AND QUALIFICATIONS REQUIRED:

Essential

  • UK GMC Registered with valid licence to practice
  • 2 years post graduate experience of working as a doctor in the UK within the NHS (minimum)

Desirable

  • 2+ Years of UK clinical experience in any specialty
  • 2+ years of psychiatry experience
  • Previous clinical research experience in SMO/CRO

RESPONSIBILITIES:

Clinical activities:

  • Fulfil the role of Sub Investigator / Principal Investigator where delegated.
  • Provision of medical care and oversight of clinical trial participants.
  • Ensure trial related procedures are completed in accordance with ICH-GCP guidelines and in compliance with the protocol.
  • Review medical records of potential study participants.
  • Remain proactive in participants study visits, including taking informed consent, physical examinations and other clinical procedures.
  • Ensure that study documentation is completed, signed off, and actioned, as appropriate.
  • Maintain accurate source notes.
  • Review medical reports and lab results.
  • Assist clinical staff members in various clinical activities as required.
  • Participate in site monitoring visits with Clinical Research Associates.
  • Ensure timelines for data queries are achieved.
  • Continuously work towards maintaining and improving quality in all areas.
  • On-call rota duties as required.
  • Assess and review memory clinic patients (only applicable to sites where MAC operates a memory clinic)

Management:

  • Attend Investigator Meetings (IM), Site Initiation Visits (SIV) and Pre-Study Selection Visits (PSSV) as required.
  • Review source documents.
  • Participate in sponsor and regulatory audits as required.
  • Participate in meetings with colleagues and customers.

Leadership

  • Provide practical help and guidance to other staff.
  • Instil confidence in patients, customers and colleagues.
  • Providing training to the clinical/ recruitment teams on essential medical information and protocols when required.

Commercial Awareness and Contribution to Targets

  • Maintain an awareness of our key customers and market competitors.
  • Share ideas from previous work environments to enhance current role.
  • Maintain an awareness of site KPI's and contribute positively to meeting these targets.

Professional development

  • Always maintain a professional attitude and appearance to customers/colleagues.
  • Ensure that GMC requirements for revalidation are met appropriately to retain license to practice.
  • Identify opportunities for self-development.

Recruitment:

  • Assist with the development of recruitment strategy with the Envision team as a therapy area specialist.
  • Maintain awareness of chat and screen fails and patient drop-out rates, taking appropriate corrective action.
  • Keep up to date with study status, ensuring each stage is optimised.
  • Establish and maintain relationships with local GPs, Consultants and service providers.

General:

  • Share experience and knowledge with colleagues as appropriate and in an appropriate manner.
  • Compliance with MAC policy on equality and diversity
  • To maintain professional qualifications required for the role, including continuous personal development
  • To work to the requirements of SI 2004 no 1031 and amendments thereof, which includes Good Clinical Practice
  • To work according to MAC SOPs, guidelines and policies
  • To work according to current data protection standards and practice good information management. Maintenance of strict confidentiality of patient and business-related data.
  • To maintain a high level of initiative and personal responsibility, liaising appropriately with team members and managers to ensure your job role is efficiently carried out
  • To support the aims of MAC and to represent MAC appropriately in a professional way to all our customers

PHYSICAL, WORK ENVIRONMENT, TRAVEL DEMANDS:

  • Dealing with bodily fluids.
  • Long periods looking at a computer screen.
  • Meeting deadlines and working within strict timelines.
  • Ability to travel between sites if required.
  • Ability to travel to national/international meetings.

BENEFITS:

  • Health Insurance
  • Eye Care Vouchers
  • Cycle to work scheme
  • Free onsite parking
  • 25 days annual leave (increasing in increments to 30 days after 6 years' service)
  • Your birthday off work

MAC Clinical Research invites applications from highly motivated candidates, with a desire to fulfil their full potential. You will be working with an organisation that sees you as an investment and is keen for you to achieve your career aspirations.

Please email should you require any special arrangements or reasonable adjustments to be made throughout this selection process. This will enable us to accommodate your request as necessary.

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