Clinical Study Coordinator CV-Library Clinical Study Coordinator

Scienceabode; Bracknell, Basingstoke; Hybrid; GBP 60,000 - 80,000; Full time

Job summary

A leading pharmaceutical company is hiring a Clinical Study Coordinator in Bracknell. This contract role requires negotiation skills and previous affiliate experience. You will collaborate on timelines and compliance while managing contracts and regulatory submissions. The position allows remote work three days a week and requires entitlement to work in the UK. Attractive hourly rates between £14.68 and £19.39 are offered, with the need for candidates to potentially undergo a DBS check.

Qualifications

• Must hold a relevant scientific degree or have equivalent working experience.
• Essential to have previous affiliate and/or finance experience.
• Experience in contract creation and negotiation is required.
• Knowledge of regulations pertaining to medical research is necessary.
• Must understand the clinical drug development process.

Responsibilities

• Negotiate and obtain fully executed contracts and track trial compliance.
• Ensure costs, timeline, and risk management are monitored.
• Forecast timelines and financial metrics with affiliates.
• Provide regulatory documents to investigators for submission.
• Manage study through to final deliverables.

Skills

Contract creation and negotiation

Financial experience

Regulatory knowledge

Clinical drug development understanding

Education

Relevant scientific degree or equivalent experience

Job description

CK Group are recruiting for a Clinical Study Coordinator to join a company in the pharmaceutical industry on a contract basis for 12 months.

Salary: £14.68 to £19.39 per hour PAYE

Clinical Study Coordinator Role:

• Negotiate and obtain fully executed contracts as well as contract amendments and track trial compliance.
• Ensure that costs, timeline, scope, and risk management process are in place to monitor and measure performance.
• Forecast timelines and financial metrics by liaising with the affiliates and/or Investigator to obtain the latest financial and milestone/enrolment data.
• Collate and provide applicable regulatory documents to investigator for submission.
• Manage study through final deliverables.
• Oversight of clinical supply requests, feasibility, and forecasting.

Your Background:

• Hold a relevant scientific degree or have equivalent working experience.
• Previous affiliate and/or finance experience such as processing of invoices or PO set-up essential.
• Contract creation and negotiation experience.
• Knowledge of regulations and guidelines that apply to the conduct of medical research.
• Understanding of the clinical drug development process.

Company:

Our client is one of the largest pharmaceutical companies in the world. They focus on finding answers for some of the world's most urgent medical needs.

Location:

This role can be based at our client's site in either Bracknell or Basingstoke 3 days per week, with the rest remote/home working.

Apply:

For more information, or to apply for this Clinical Study Coordinator role, please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (Apply online only). It is essential that applicants hold entitlement to work in the UK. Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.

£14.68 – £19.39/hour

Apply Online