Regulatory Submissions (Study Start-up) Manager
Medpace is seeking a Study Start-up Manager to join their Clinical Operations team in Singapore. The role involves managing global study start-up activities, performing quality checks on submission documents, and reviewing regulations to solve project challenges. Candidates should have over 5 years of experience in clinical research, preferably at a CRO. This position requires strong communication skills to handle bid defenses, meetings, and audits.
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Experience
5+ years
Function
Operations
Work mode
Onsite, Singapore
Company
Tier 2
What you will work on
Medpace is seeking a Study Start-up Manager to join their Clinical Operations team in Singapore. The role involves managing global study start-up activities, performing quality checks on submission documents, and reviewing regulations to solve project challenges. Candidates should have over 5 years of experience in clinical research, preferably at a CRO. This position requires strong communication skills to handle bid defenses, meetings, and audits.
TAL's take
Solid role at an established CRO, though lacking specific technical stack requirements and clear management scope.
Clear and coherent responsibilities related to clinical study start-up and regulatory submissions.
Must haves
- 5+ years of experience in clinical research
- Strong oral and written communication skills
- Experience with submission documents and site essential documents
- Ability to review pertinent regulations
About the company
Medpace is an established global clinical contract research organization with significant industry presence.