Clinical Trials Manager / Hybrid Work - Pioneer Data Systems
West Chester, PA 19380
About the Job
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
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
Source : Pioneer Data Systems