Medical affair associate Work, Jobs in London (with Salaries)

Drug Safety Associate II
Corbus Pharmaceuticals Inc —London
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Nursing
Quick apply
Associate Medical Director / Medical Director
JPA Health —London
- Full-time
- Doctoral degree
- Travel
- AI
Quick apply
Residence Life Coordinator, First Year Focus - NYU London
New York University —London
- Weekend availability
- Customer service
- University
- No degree
- Annual leave
School Leaver Tax Associate (ATT) – VAT Tax - September 2026 - London
PKF Littlejohn —London
- Full-time
- Bachelor's degree
- No degree
- Annual leave
Associate Director, Medical Programs
Nucs AI —London
- Full-time
- Hybrid work
- Master's degree
- Project management
- Bachelor's degree
Quick apply
International HEOR & HTA Associate Director, NS
Novartis —London
- £69,440 - £128,960 a year
- Full-time
- Hybrid work
- Doctoral degree
- Data analysis skills
- English
3d
Clinical Trials Manager
Gilead Sciences —London
- Full-time
- Management
- Doctoral degree
- Master's degree
International HEOR & HTA Associate Director, Oncology
Novartis —London
- £69,440 - £128,960 a year
- Full-time
- Hybrid work
- Doctoral degree
- Data analysis skills
- English
3d
CMC Associate Director
Androlabs —London
- £85,000 - £108,000 a year
- Full-time
- Hybrid work
- Management
- Project management
- IT
- Annual leave
Quick apply
10d
Tax Associate (ATT) – Indirect Tax - September 2026 - London
PKF Littlejohn —London
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Outlook
- Annual leave
Manager for Academic Affairs - NYU London
New York University —London
- Full-time
- Computer literacy
- Microsoft Office
- Computer skills
- Annual leave
Associate Director, IMACE Scientific Content, NS
Novartis —London
- £67,900 - £126,100 a year
- Full-time
- Hybrid work
- Doctoral degree
- English
- Organisational skills
2d
Associate Director, Medical Affairs
Gilead Sciences —Uxbridge
- Full-time
- Doctoral degree
- Analysis skills
- Travel
2d
Senior Regulatory Associate
Pfizer —Walton-on-Thames
- Full-time
- Doctoral degree
- Marketing
- Computer literacy
4d
Principal Regulatory Affairs Specialist (UK, IVDR) Remote UK
Cepheid —Amersham
- Full-time
- Remote
- Master's degree
- Bachelor's degree
- Annual leave
9d
Associate Director, Global Medical Affairs (2-year contract)
BioNTech AG —London
- Full-time
- Doctoral degree
- Project management
- Travel
8d
Head of Study, Site Management and Monitoring
Ipsen Biopharm Ltd —London
- Full-time
- Doctoral degree
- English
- Master's degree
Senior Regulatory Specialist
Androlabs —London
- £85,000 - £108,000 a year
- Full-time
- Hybrid work
- IT
- Annual leave
Quick apply
10d
Engagement Consultant
WSP —London
- Part-time
- Hybrid work
- English
- No degree
- Organisational skills
- Flexitime
- Work from home
11d
Enterprise Risk Management (ERM) Senior Associate
Pwc UK —London
- Full-time
- Analysis skills
- Project management
- Presentation skills

I want to receive the latest job alerts for medical affair associate in london

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Drug Safety Associate II

Corbus Pharmaceuticals Inc -
London

Quick apply

Job details

Qualifications

Microsoft Powerpoint
Microsoft Word
Nursing
Microsoft Excel
Oracle
Doctoral degree
Microsoft Office
Master's degree
Bachelor's degree
Technical writing
ESG
FDA regulations
Nursing

Full job description

Description:

The Drug Safety Associate II/Senior Drug Safety Associate is the senior technical contributor anchoring Corbus Pharmaceuticals' in-house PV function. In addition to managing complex ICSRs and SUSARs, this individual will assist with case processing, QC of cases, SMP authoring, generate listings upon request, assist with aggregate report preparation (DSUR/PBRER), Literature search, and mentor the junior associate. The ideal candidate brings deep Veeva Vault Safety expertise and thorough command of FDA and EMA PV regulations.

KEY RESPONSIBILITIES

Complex Case Management:

Independently process and quality-review complex ICSRs, SUSARs, and cases of special interest across all Corbus programs.
Lead SUSAR causality assessment and blind review with the Medical Monitor; coordinate unblinding decisions per protocol.
Perform and document expectedness assessment against the Reference Safety Information (IB/SmPC);
Oversee 7- and 15-day expedited submission workflow; act as backup submitter and regulatory gateway owner.
QC case quality and narratives prepared by the junior associate; provide coaching and sign-off.

Aggregate Reporting & Signal Detection:

Maintain Safety meeting minutes, documentation for Signal detection and Safety trackers
Generate ad hoc line listings and cumulative summaries for regulatory queries using Vault Safety analytics.

Regulatory Collaboration & Audit Readiness:

Regular Safety SOP review, assist in drafting and maintaining the Pharmacovigilance System Master File (PSMF) and procedural documents (SOPs, work instructions, templates) as needed.
Assist with PV audit and inspection preparation; respond to agency queries and manage post-inspection CAPAs.
Manage PV agreements (PVAs) with CRO and licensing partners; ensure compliance with contractual safety exchange timelines.
Represent PV on cross-functional teams (Clinical, Regulatory, Medical Affairs); provide safety input into protocol amendments and IBs.

System Ownership & Team Development:

Serve as functional administrator for Veeva Vault Safety: configure workflows, manage user access, and coordinate validation with IT.
Oversee Safety-EDC reconciliation between Vault Safety and Veeva EDC for ongoing trials.
Mentor and train the junior Drug Safety Associate; conduct case-level QC and provide structured development feedback.

Requirements:

QUALIFICATIONS

Required:

Bachelor's degree in Pharmacy, Nursing, Life Sciences, or a related discipline; Master's, PharmD, or RN strongly preferred.
5+ years of progressive pharmacovigilance experience in the pharmaceutical, biotech, or CRO industry.
Demonstrated proficiency in Veeva Vault Safety or Oracle Argus for end-to-end case processing and reporting.
Hands-on experience authoring DSURs and/or PBRERs; strong technical writing skills.
Deep knowledge of ICH E2A, E2B(R3), E2C, E2D, E2E, FDA 21 CFR Part 312, and EMA GVP Modules I–IX.
Expert-level MedDRA coding; experience with signal detection methodologies.
Track record of direct regulatory interactions and safety committee participation.

Preferred:

Experience in Oncology therapeutic area.
Prior sponsor-side experience at a small or mid-size biotech.
PSMF authoring and GVP Module VII experience.
E2B electronic gateway submissions (FDA ESG, ASK-EudraCT, VigiBase).
Veeva Vault Safety administrator or system validation experience.

TECHNICAL SKILLS:

Veeva Vault Safety — case processing, workflow configuration, analytics, and E2B gateway management.
MedDRA (expert-level) and WHODrug Global coding.
Microsoft Office — advanced Excel for data analysis; Word/PowerPoint for regulatory documents.
Document management systems (Vault QMS or equivalent) for SOP and PSMF maintenance.

Corbus Culture:

Corbus is a close-knit global team of high-achieving, innovative, creative and, above all else, passionate employees. We hire for personality as well as for skill. At Corbus, we take pride in our “family” atmosphere where each person’s contribution is vital to our success. As a Corbus employee, you are empowered to think creatively and be proactive in your approach. There is no place for politics or red tape here.

About Corbus:

Corbus Pharmaceuticals Holdings, Inc. is a clinical-stage biotechnology company focused on developing innovative therapies in oncology and obesity. Our mission is to help people defeat serious illness by advancing differentiated scientific approaches targeting well-understood biological pathways with significant unmet medical need. Corbus’ lead oncology program, CRB-701, is a next-generation antibody-drug conjugate (ADC) targeting Nectin-4-expressing tumors and is being developed for multiple solid tumor indications. Our obesity program, CRB-913, is a highly peripherally restricted CB1 receptor inverse agonist designed to support meaningful weight loss while minimizing central nervous system side effects. Together, these programs reflect our commitment to advancing transformative therapies through rigorous science and clinical innovation.

Headquartered in Norwood, Massachusetts, Corbus fosters a collaborative, entrepreneurial environment where employees are empowered to make meaningful contributions and help shape the future of the company. For more information, visit corbuspharma.com and connect with us on LinkedIn. Corbus Pharmaceuticals Holdings, Inc. is an equal opportunity employer.

Quick apply

Refine Your Search

medical affair associate jobs in london

Drug Safety Associate II

Associate Medical Director / Medical Director

Residence Life Coordinator, First Year Focus - NYU London

School Leaver Tax Associate (ATT) – VAT Tax - September 2026 - London

Associate Director, Medical Programs

International HEOR & HTA Associate Director, NS

Clinical Trials Manager

International HEOR & HTA Associate Director, Oncology

CMC Associate Director

Tax Associate (ATT) – Indirect Tax - September 2026 - London

Manager for Academic Affairs - NYU London

Associate Director, IMACE Scientific Content, NS

Associate Director, Medical Affairs

Senior Regulatory Associate

Principal Regulatory Affairs Specialist (UK, IVDR) Remote UK

Associate Director, Global Medical Affairs (2-year contract)

Head of Study, Site Management and Monitoring

Senior Regulatory Specialist

Engagement Consultant

Enterprise Risk Management (ERM) Senior Associate

I want to receive the latest job alerts for medical affair associate in london

Related Searches

Explore jobs in more locations

Jobseeker tools

Employer Tools

Browse

Stay Connected