7 years relevant experience in scientific or clinical environment
Strong negotiation and communication skills
In-depth knowledge of drug development process
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IQVIA Inc is seeking a Study Start Up Manager to oversee site activation, maintenance, and regulatory activities for clinical studies. The role requires significant experience in a scientific or clinical environment and offers competitive compensation and benefits.
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Job Summary
The role involves directing and managing the delivery of site activation, maintenance, and regulatory activities for selected studies or multi-protocol programs.
Candidates must possess a Bachelor's Degree in Life Sciences and at least 7 years of relevant experience in an international scientific or clinical environment.
The position offers a potential base pay range of $103,000.00 to $153,000.00 annually, depending on qualifications and location.
Matching Summary
Match Score: 75
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IQVIA Inc is seeking a Study Start Up Manager to oversee site activation, maintenance, and regulatory activities for clinical studies. The role requires significant experience in a scientific or clinical environment and offers competitive compensation and benefits.
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Salary
Base: $103,000.00 - $153,000.00 annualized; Bonus/Equity: Incentive plans and bonuses may be offered; Benefits: Range of health, wellness, and other benefits available
Skills & Requirements
Must-have
7 years relevant experience in scientific or clinical environment
Strong negotiation and communication skills
In-depth knowledge of drug development process
Proficiency in CTMS and project tracking tools
Thorough understanding of GCP and ICH guidelines
Nice-to-have
Ability to challenge and offer creative solutions
Experience mentoring and coaching colleagues
Proven ability to work through others on complex projects
Good presentation skills for clients and professional bodies
Key Requirements
Bachelor's Degree in Life Sciences or related field
7 years' relevant experience in scientific or clinical environment
Demonstrable experience in an international role
Strong knowledge of Clinical Practice (GCP) and ICH guidelines