Senior Associate, Clinical Operations
Scientific Search - Norwalk, Connecticut, us, 06860
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Overview
Associate Study Manager, Clinical Operations
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Join our client as an Associate Study Manager, Clinical Operations. You will play a critical role in leading the operational planning and execution of translational research studies, ensuring compliance with regulatory standards, and collaborating with cross-functional teams to deliver high-quality data on time and within budget. As a key member of our Clinical Operations team, you will have the opportunity to make a meaningful impact on the lives of multiple myeloma patients and contribute to the advancement of our mission. Location: Norwalk, CT/Remote (hybrid)
Summary
Join our client as an Associate Study Manager, Clinical Operations. You will play a critical role in leading the operational planning and execution of translational research studies, ensuring compliance with regulatory standards, and collaborating with cross-functional teams to deliver high-quality data on time and within budget. As a key member of our Clinical Operations team, you will have the opportunity to make a meaningful impact on the lives of multiple myeloma patients and contribute to the advancement of our mission.
Why You Should Apply
Competitive salary range: $80,000 - $110,000 per year Opportunity to work on high-impact projects that drive innovation and progress in multiple myeloma research Collaborative and dynamic work environment with a team of dedicated professionals Professional development opportunities to advance your career in clinical research
What You’ll Be Doing
Manage all aspects of study execution, including protocol development, feasibility assessments, site selection, and budget planning Oversee study design, planning, and execution, including writing and reviewing study protocols and informed consent forms Manage study budgets, track expenses, and prepare study reports Collaborate with cross-functional teams to ensure study progress and compliance with regulatory standards Identify and mitigate potential risks associated with studies Develop and facilitate requests for proposals (RFPs) for study vendors
About You
Bachelor's degree in scientific or healthcare discipline required; master's degree preferred Minimum of 5 years of pharmaceutical, biotech, academic, or CRO related/oncology clinical study operations experience Experience working with Contract Research Organizations (CROs) and/or other external vendors Strong leadership skills and ability to manage study teams and external vendors effectively Excellent communication and organizational skills Ability to travel as necessary (approximately 10%)
How To Apply
We’d love to see your resume, but we don’t need it to have a conversation. Send us an email to Emily@scientificsearch.com and tell me why you’re interested. Or, feel free to email your resume. Please include Job#19370.
Seniority level
Seniority level Mid-Senior level Employment type
Employment type Full-time Job function
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