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Associate Clinical Project Manager

Stevenage, HertfordshirePermanent
£48,000 - £68,000 per annum
Job Reference: J5634729
Updated On: 19/05/2021
Status: Open to Applications
Hyper Recruitment Solutions
Sectors: IS&T

Skills: Clinical - Clinical Project Management (Perm), Clinical - Clinical Project Management (Contract), Clinical - Clinical Coordinator

Job Information

Role Overview

We are currently looking for an Associate Clinical Project Manager to join a leading CRO based in the London area on a 12 month contract. As the Associate Clinical Project Manager you will be responsible for the execution of all assigned studies and initiatives that generate genotyping data and identify patients within specific genetic subsets to support interventional trials.

Key Duties and Responsibilities

Your duties as the Associate Clinical Project Manager will be varied however the key duties and responsibilities are as follows:

1. Supporting for the oversight and day-to-day management of global genotyping activities and ensuring the planning, implementation, coordination and reporting of genotyping initiatives are in line with the corporate objectives

2. Monitoring the progress of studies, identify study-related trends/issues and work with the Clinical Operations/genotyping team to implement corrective actions when necessary


3. Supporting and monitoring CRO and third-party vendor activities, including Investigator contract/budgets, document management, study set-up, project management


4. Contributing to the preparation, design and/or review of essential study documents, ethics and other required local/national submission requirements

5. Ensuring study certifications, insurance, licenses and registrations are maintained where appropriate

Role Requirements

To be successful in your application to this exciting opportunity as the Associate Clinical Project Manager we are looking to identify the following on your profile and past history:

1. Relevant degree in Life Sciences or equivalent

2. Proven industry experience in pharmaceutical or biotech industry (including CRO) working in the management of clinical trials

3. Have the ability to proficiently represent the Clinical Operations Dept across all functions as well as external parties and KOLs

4. Ophthalmology experience would be beneficial



Key Words: Clinical Project Manager / GXP / ATMP / GMO/ Biologics handling
Kayleigh Wells
Your Recruitment ConsultantKayleigh WellsKayleigh.wells@hyperec.com
DisclaimerHyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for our talent development. We welcome applications for any applicant who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment processionals and scientists. We look forward to helping you with your next career moves.