Medpace
From Medpace's careers page
Status: listed on the employer's own careers page when we last checked (daily). Confirm on their site before applying.
Our corporate activities are growing rapidly, and we are currently seeking a full-time Associate Clinical Data Manager to join our Data Management team in our Mumbai office. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.
Develop and maintain Data Management Plan
Oversee development and maintenance of CRF specifications, CRF completion guidelines, edit check specifications, and external database specifications
Oversee EDC design, development, validation
Manage multiple projects, timelines, and Data Management teams to ensure quality and timely deliverables
Develop project metrics and reports to support data-driven decision-making
Represent Data Management in sponsor meetings and cross-functional discussions
Coordinate overall Data Management by serving as the primary contact for the Sponsor, external data providers and all project team members
Bachelor’s degree with 5+ years of clinical Data Management experience, including managing multiple clinical projects and serving as the primary sponsor contact.
Prior experience in line management, team and project leadership, and Data Management deliverables
Strong understanding of clinical Data Management processes, database structures, and clinical research methodologies.
Proficiency with EDC, Excel, and data analysis tools (experience with Rave or SAS preferred)
Working knowledge of medical terminology and clinical research concepts
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
Medpace Perks
Flexible work environment
Competitive compensation and benefits package
Competitive PTO packages
Structured career paths with opportunities for professional growth
Company-sponsored employee appreciation events
Employee health and wellness initiatives
Awards
Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
Develop and maintain Data Management Plan
Oversee development and maintenance of CRF specifications, CRF completion guidelines, edit check specifications, and external database specifications
Oversee EDC design, development, validation
Manage multiple projects, timelines, and Data Management teams to ensure quality and timely deliverables
Develop project metrics and reports to support data-driven decision-making
Represent Data Management in sponsor meetings and cross-functional discussions
Coordinate overall Data Management by serving as the primary contact for the Sponsor, external data providers and all project team members
Bachelor’s degree with 5+ years of clinical Data Management experience, including managing multiple clinical projects and serving as the primary sponsor contact.
Prior experience in line management, team and project leadership, and Data Management deliverables
Strong understanding of clinical Data Management processes, database structures, and clinical research methodologies.
Proficiency with EDC, Excel, and data analysis tools (experience with Rave or SAS preferred)
Working knowledge of medical terminology and clinical research concepts
Scores your resume against this job the way resume scanners do: the job's hard and soft skills, searchability, recruiter tips and formatting.
Create a free account to see your score. Your resume stays in this browser until then, and we never store it.
Already a member? Sign in