Study Start up Submissions Manager

Medpace Inc. looking forStudy Start up Submissions Manager to join our dynamic team and embark on a rewarding career journey"

We are currently seeking a full-time, office-based Study Start up Submissions Manager to join our Clinical Operations team in India.

Responsibilities

• Efficiently manage and successfully execute all aspects of local and global start-up;
• Independently interact with Sponsor, sites, Institutional Review Boards (IRBs)/Ethics Committees (ECs) and regulatory agencies (minimum DCGI);
• Perform quality checks on submission documents and site essential documents;
• Prepare and approve informed consent forms;
• Review pertinent regulations to develop proactive solutions to start-up issues and challenges; and
• Present during bid defenses, general capabilities meetings, and audits.

Qualifications

• Bachelors degree and more than 8 years of regulatory submissions experience in clinical research, preferably with a CRO. Experience may include CRA or project management experience;
• Local and Regional experience will be highly advantageous; and
• Strong oral and written communication skills.

Medpace Overview

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work weve 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

• Hybrid work-from-home options (dependent upon position and level)
• Competitive PTO packages
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives
• Flexible work schedule
• Competitive compensation and benefits package
• Structured career paths with opportunities for professional growth