Clinical Trials Manager / Hybrid Work

Full Job Description

Position Details:

Our client, a world-leading Pharmaceutical Company in West Chester, PA is currently looking for a Clinical Trials Manager join their expanding team.

Job Title: Clinical Trials Manager / Hybrid Work

Duration: 12 months contract, extendable up to 24 months

Location: West Chester, PA

Hybrid. 3 days in office and 2 from home.

Note:

The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.

You may participate in the company group medical insurance plan

Job Description:

Will Operational support for Global Medical Affairs, Governance, oversight and operational support

Review milestones, review and support entry and information to track clinical studies

Ensure inspection readiness of clinical studies

Help local study team's start-up their studies

Work with sites, get start up documents, set up monitoring plans

Must have experience with Clinical Trials and studies around SOP development & review

Regulatory and quality inspection readiness experience

Medical affairs experience in the post marketing study phase experience Ideal

Clinical Trial Manager / Clinical Project Manager/ Clinical Project Manager with regulatory experience will be an Ideal fit

Study oversight, start-up and tracking

Qualifications:

3-5 years of experience

BA/BS in life sciences will be ideal, Advanced degree a plus

Daily engagement with local study leads, Sr. Global Managers tracking day to day clinical activities

Must have experience in clinical study start-ups

Veeva Experience a plus

Experience in CTMS including Veeva Masterfile helpful

Position will revolve around Post approval trials

Candidates will early clinical trial experience without Medical affairs experience will also be considered