QA (GCP) Opportunities - contract in City of London

Job description

I'm currently connecting with freelance QA professionals who have experience in Good Clinical Practice (GCP) for upcoming roles with clients in the clinical research, pharmaceutical, and biotech sectors.

Are you a QA professional with a solid grounding in GCP looking for your next move in the life sciences industry? I'm working closely with clients across the UK and Ireland who are consistently on the lookout for experienced professionals to support ongoing and upcoming clinical trials.

Responsibilities include:

• Oversight of GCP compliance in early to late-phase clinical trials.
• Involvement in audits and inspections (internal, external, regulatory).
• Acting as a key QA contact across cross-functional study teams.
• Supporting quality systems and continuous improvement initiatives.

Whether you're looking to join a growing biotech, a global pharma, or a niche CRO, there’s something on the horizon that could align with your goals .

Skills & Requirements

• Proven experience in a GCP QA role within clinical research or related life sciences setting.
• Hands-on involvement with audits and/or regulatory inspections (FDA, EMA, MHRA etc.).
• Solid understanding of ICH-GCP and applicable regulatory requirements.
• Strong communication and stakeholder management skills, with the ability to influence quality culture.

If you're open to hearing about future QA GCP opportunities, let's connect. Drop me a message here or send your CV to [email protected] and I’ll be in touch to discuss how we can align your experience with upcoming roles.

Extra information

Status

Open

Education Level

Secondary School

Location

City of London

Type of Contract

Casual / Part Time Jobs

Published at

21-10-2025

Full UK/EU driving license preferred

No

Car Preferred

No

Must be eligible to work in the EU

No

Cover Letter Required

No

Languages

English