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Hyper Recruitment Solutions
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Clinical Project Manager

Permanent
£57,000 - £80,000 per annum
Job Reference: J5634730
Updated On: 19/05/2021
Status: Now Interviewing
Hyper Recruitment Solutions
Sectors: IS&T

Skills: Clinical - Clinical Project Management (Contract)

Job Information

Role Overview

We are currently looking for a Clinical Project Manager to join a globally leading Biotechnology company based in the London area. As the 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 Clinical Project Manager will be varied however the key duties and responsibilities are as follows:

1. Work across all interventional trials to ensure that Study team members are able to represent the needs of the genotyping team and objectives to respective study sites, Investigators and referral networks

2. 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

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

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

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

6. Providing input into the identification and selection of genotyping investigators as per the clinical operations strategy

Role Requirements

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

1. Minimum 3 years’ experience working as a Clinical Project Manager in Phase I-IV studies within the pharmaceutical industry or a CRO

2. Extensive experience in direct management of study start up activities

3. Be an independent thinker with the ability to anticipate issues and risks and to mitigate accordingly

4. Ophthalmology experience would be beneficial




Key Words: Clinical Project Manager / Genotyping / Ophthalmology / GXP / ATMP / GMO / Biologics handling


Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development. We therefore welcome applications for any interested parties 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 professionals and scientists. We look forward to helping you with your next career moves.
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.