Genesis Global Group is currently looking for 2 Associate Project Managers to join a leading Pharmaceutical company based in Paris. Full time position with fantastic benefits available to all employees from day 1 and high competitive salaries.

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Job Functions

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You will perform delegated tasks by the Clinical Project Manager regarding the preparation, conduct and reporting of the phase I to phase IV allocated clinical trials in compliance with ICH guidelines and local/international regulations
You will review monitoring visit reports and trial deviation form; Contribute to the preparation of study documents, protocols, and other study specific documents; Update of trial reporting tools including metrics and KPIs and follow-up of CAPA progress; Completion of Trial Master Files; Budget preparation; Regulatory process; Engage with CRAs (internal and outsourced) for site monitoring oversight and issue solving; Contribute in preparation of audits and inspections; Perform other related duties as assigned.

 

Requirements

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• Medical Doctor, Pharmacist or Scientific background with bachelor or master degree

• Experience of monitoring clinical studies as a Lead CRA or Associate PM in a pharmaceutical or CRO laboratory

• 6 years of clinical development experience (phase II and III)

• Experience in oncology or in autoimmune inflammatory pathologies would be an advantage

• Control of the regulatory environment of clinical trials

• Fluent professional English mandatory

Additional information

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• Permanent position available immediately

• Position based in Paris

• Package to define according to experience

• English speaking role, no French required

• Interviews to take place immediately

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In order to apply for this role, please forward your most up to date CV and quote the reference number.

 

 

TAGS: Clinical Studies, Oncology, CRO, Clinical Development, Clinical Projects