Clinical Trial Expert Role
We are seeking a Clinical Trial Expert to join our team on a contract basis for 12 months.
* Contribute to specific study strategies with a strong background in trial execution.
* Establish and maintain relationships with key internal partners, stakeholders, and external partners.
* Support the quality of clinical trials by participating in audits and inspection readiness throughout the study lifecycle.
* Lead the implementation of systems maintenance, tools, and reports required across the clinical trial life cycle (eCOA, IxRS etc).
* Contribute to the development and maintenance of relevant study oversight documentations/charters.
* Track clinical study progress and address issues in collaboration with study teams, affiliates, sites, and CROs as appropriate.
Requirements:
* A growth mindset and enthusiasm for learning through experience.
* Comfortable thinking on your feet and thriving in fast-paced, ambiguous, and highly collaborative environments.
* Experience in the pharmaceutical and/or healthcare industry and drug development.
* A university degree or equivalent years of experience, preferably in life sciences.
* A strong working knowledge of the drug development process and respective regulations.
* Comfortable traveling internationally based on specific program needs.
* Experience in healthy volunteer studies and study close-outs is essential.
About Us:
Our client is a world-leading biopharmaceutical company discovering, developing, and providing over 160 different medicines, vaccines, and consumer healthcare products to improve lives worldwide.
Location:
This role is based at our client's site in Welwyn Garden City, requiring 2-3 days per week on-site and remote work for the remainder of the week.
Application Instructions:
Please ensure you hold entitlement to work in the UK. This role may be subject to a satisfactory DBS check. If this position isn't suitable, but you're interested in new roles, follow us on LinkedIn (CKA-Group) for the latest jobs and company news.