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Lifelancer
Study Start Up Manager
Remote · Parsippany, New Jersey, United States · Full time · Mid level
$74.6k–$216k / year
About the role
Manage site activation, maintenance, and regulatory activities for clinical studies. Oversee multi-protocol programs ensuring compliance and project delivery.
What you’ll do
• Oversee site activation and maintenance per project timelines. • Develop and maintain management plans and project strategies. • Provide regulatory and scientific support for clinical trials. • Ensure quality standards and compliance during site activation. • Mentor colleagues and manage project documentation.
What you’ll bring
• Bachelor's degree in life sciences or related field. • 7 years relevant scientific or clinical experience. • Strong negotiation and communication skills. • Knowledge of GCP, ICH, and regulatory guidelines. • Work authorization for United States.
Life at Lifelancer
Offers health and welfare benefits, incentive plans, bonuses, and a supportive work environment.
About Lifelancer
Lifelancer connects talent with opportunities in pharma, biotech, health sciences, healthtech, and IT domains.