221 Senior Pharmacovigilance Scientist jobs in the United Kingdom

• Conduct signal detection and evaluation activities for assigned pharmaceutical products.
• Perform aggregate safety data review and analysis, including periodic safety update reports (PSURs) and development safety update reports (DSURs).
• Author and review safety narratives for regulatory submissions and internal reports.
• Contribute to risk management plans (RMPs) and risk-benefit assessments.
• Ensure timely and accurate processing of adverse event reports in compliance with global regulatory guidelines (e.g., GVP, FDA).
• Collaborate with clinical development, regulatory affairs, and medical affairs teams to ensure integrated safety monitoring.
• Liaise with regulatory authorities and external partners regarding safety matters.
• Maintain knowledge of global pharmacovigilance regulations and guidelines.
• Participate in the development and improvement of pharmacovigilance processes and systems.
• Mentor and provide guidance to junior pharmacovigilance staff.

• Advanced degree (e.g., M.D., Pharm.D., Ph.D., M.Sc.) in a life science, pharmacy, or related healthcare field.
• A minimum of 5 years of experience in pharmacovigilance or drug safety, with a strong understanding of regulatory requirements.
• Demonstrated experience in signal detection, safety data analysis, and aggregate reporting.
• Proficiency in safety databases (e.g., Argus, ARISg) and medical coding dictionaries (e.g., MedDRA, WHODrug).
• Excellent written and verbal communication skills, with the ability to articulate complex scientific and regulatory information clearly.
• Strong analytical and problem-solving abilities.
• Ability to work independently and manage multiple projects simultaneously in a remote setting.
• Experience in preparing regulatory safety documents is highly desirable.
• Knowledge of clinical trial processes is a plus.
• Detail-oriented with a commitment to accuracy and compliance.

Job Title: Clinical Research Coordinator (Band 6 Nurse)

Contract Type: Part-Time (2–3 days/week)

Overview:

We are seeking a skilled and motivated Band 6 Nurse to support clinical research activities as a Clinical Research Coordinator. This part-time role offers an excellent opportunity to contribute to impactful research while maintaining a flexible schedule.

Key Responsibilities:

• Identify and recruit eligible patients for clinical trials.
• Perform accurate and timely data entry into study databases.
• Collaborate with research and clinical teams to ensure protocol compliance.
• Maintain high standards of documentation and regulatory adherence.

Requirements:

• Registered Band 6 Nurse with relevant clinical experience.
• Demonstrated experience in patient identification and data entry.
• Strong attention to detail and organizational skills.
• Must be available to work every Wednesday, plus two additional weekdays.

Please submit your CV or get in touch via email:

Our client, an innovative clinical research organisation (CRO) is currently looking for a Clinical Research Physician to join their team in London.

As a Clinical Research Physician, you will spearhead early stage clinical trials, manage study protocols and ensure ethical conduct and compliance at all stages. You will collaborate with an expert sponsor team and contribute to ground-breaking projects that advance healthcare and improve patient outcomes.

You will be driven to enhance patient safety, improve quality systems and ensure the data produced for the development of individual drugs is of the highest standard.

This role will offer tremendous scope for leadership and personal development. With this site being relatively new, this person will have the remit to grow and nurture a clinical research team around them as well as having significant involvement and influence with their sponsors.

Key Responsibilities

• Provide medical direction, oversee protocol compliance and ensure participant safety throughout clinical trials.
• Evaluate and interpret clinical data, performing necessary assessments to maintain data accuracy and integrity.
• Collaborate on scientific feasibility for new inquiries, assisting sponsors and guiding clinical operations teams as needed.
• Ensure adherence to regulatory requirements and Good Clinical Practice standards, maintaining rigorous documentation and participant confidentiality.

Requirements

• A medical degree (MD) - essential
• Full and current GMC registration - essential.
• Strong background in clinical research / clinical trials.
• Proven experience as a Clinical Research Physician.
• Strong knowledge of regulatory guidelines.
• Excellent organisational, communication and analytical skills.

Park Street People Ltd is an Equal Opportunities Employer. We do not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and comply with all relevant UK legislation. We are acting as an Employment Agency in relation to this role.

Our client, an innovative clinical research organisation (CRO) is currently looking for a Clinical Research Physician to join their team in London.

As a Clinical Research Physician, you will spearhead early stage clinical trials, manage study protocols and ensure ethical conduct and compliance at all stages. You will collaborate with an expert sponsor team and contribute to ground-breaking projects that advance healthcare and improve patient outcomes.

You will be driven to enhance patient safety, improve quality systems and ensure the data produced for the development of individual drugs is of the highest standard.

This role will offer tremendous scope for leadership and personal development. With this site being relatively new, this person will have the remit to grow and nurture a clinical research team around them as well as having significant involvement and influence with their sponsors.

Key Responsibilities

• Provide medical direction, oversee protocol compliance and ensure participant safety throughout clinical trials.
• Evaluate and interpret clinical data, performing necessary assessments to maintain data accuracy and integrity.
• Collaborate on scientific feasibility for new inquiries, assisting sponsors and guiding clinical operations teams as needed.
• Ensure adherence to regulatory requirements and Good Clinical Practice standards, maintaining rigorous documentation and participant confidentiality.

Requirements

• A medical degree (MD) - essential
• Full and current GMC registration - essential.
• Strong background in clinical research / clinical trials.
• Proven experience as a Clinical Research Physician.
• Strong knowledge of regulatory guidelines.
• Excellent organisational, communication and analytical skills.

Park Street People Ltd is an Equal Opportunities Employer. We do not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and comply with all relevant UK legislation. We are acting as an Employment Agency in relation to this role.

URGENT HIRING: Clinical Research Coordinator – Bath

I'm reaching out with an exciting full-time opportunity for a Clinical Research Coordinator (CRC) to join a global clinical research service provider supporting multiple sponsors.

Therapeutic Area: Atopic Dermatitis (experience required)

Location: On-site in Bath

Start Date: ASAP

Duration: Until October (potential to extend)

This role is ideal for a Band 5/6 Nurse or Clinical Research Nurse ready to step into a CRC title.

Key Responsibilities:

• Patient identification & chart reviews
• Referral physician networking
• Community outreach

Preferred Experience:

• Background in nursing or clinical research
• Familiarity with Millennium Sauna or other EDC systems

Are you a passionate CRA II or Senior CRA looking for your next challenge?

We have an exciting, exclusive opportunity for an experienced Clinical Research Associate to join our clients newly established FSP team, working exclusively with a leading Pharmaceutical client.

This is a unique opportunity to be part of a dynamic and supportive environment where your contributions directly impact the future of medicine. Our clients FSP model provides the stability and support of a dedicated team, while you gain exposure to the innovative research of a top-tier pharmaceutical company.

About the role:

As a CRA II or Senior CRA, you will be responsible for the full range of monitoring activities, from site initiation to close-out. You'll ensure the highest standards of data quality and compliance with ICH-GCP, protocols, and all applicable regulations. This role is home-based and will involve travel to sites across your designated region.

What our client offer:

• Salary: £45,000 - £55,000 per annum, depending on experience.
• Car/Car Allowance: A company car or a competitive car allowance.
• Bonus & Benefits: An attractive bonus scheme and a comprehensive benefits package.
• Career Growth: We are committed to your professional development and offer extensive training, mentorship, and opportunities for progression within our growing FSP.

Location:

This is a home-based role to be based in one of the following regions:

• North England
• North West England
• Midlands
• London
• South England

Requirements:

• Proven experience as a CRA, with a strong understanding of the clinical trial lifecycle. 18 months minimum as a CRA to be CRAII and 3 year + to be considered for Senior CRA.
• Excellent knowledge of ICH-GCP guidelines and relevant regulations.
• Strong communication and interpersonal skills.
• A proactive and independent approach to your work.
• A full UK driving licence and willingness to travel.

If you are ready to take the next step in your career and join a company that values growth, training, and support, we want to hear from you.

Apply now or message us for more details!

#CRA #ClinicalResearch #ClinicalResearchAssociate #SeniorCRA #CRAJobs #PharmaJobs #FSP #LifeSciences #Hiring #ClinicalTrials #UKJobs#CCS-Global

Job Title: Freelance Clinical Research Associate – Associate Level (Oncology)

Location: Hybrid UK Based

Employment Type: Freelance

Function: Clinical Operations

Therapeutic Area: Oncology

Reports To: Clinical Operations Manager

About the Role

We are seeking a motivated and detail-oriented Freelance Clinical Research Associate (Associate Level) with a passion for oncology clinical trials. This is an exciting opportunity for an early-career CRA to gain hands-on experience in a dynamic, cross-functional research environment. You will support clinical trial activities across multiple oncology study sites, ensuring compliance with regulatory guidelines, ICH-GCP, and study protocols.

Key Responsibilities

• Conduct site monitoring visits (pre-study, initiation, routine, and close-out) for oncology clinical trials in accordance with study protocols and regulatory requirements.
• Assist in site selection and feasibility assessments.
• Ensure proper documentation and timely resolution of site issues.
• Support site staff in understanding and complying with study protocols and GCP guidelines.
• Verify source data and case report forms (CRFs) for accuracy, completeness, and consistency.
• Ensure timely collection and review of essential regulatory documents.
• Track patient recruitment and retention efforts at assigned sites.
• Participate in CRA training sessions, project team meetings, and sponsor meetings as required.
• Maintain high-quality communication with clinical sites and sponsor/CRO teams.
• Escalate site performance or compliance issues as needed.

Required Qualifications

• Bachelor’s degree or higher in Life Sciences, Nursing, Pharmacy, or a related field.
• Minimum of 1–2 years of clinical research experience (internships or study coordinator experience may be considered).
• Exposure to oncology trials (academic, site, or CRO experience).
• Understanding of ICH-GCP guidelines and regulatory requirements.
• Strong organizational skills with attention to detail.
• Ability to manage multiple tasks and priorities independently.
• Excellent communication and interpersonal skills.
• Proficiency with clinical trial management systems (CTMS), EDC systems, and Microsoft Office.