Scholar Rock is hiring a
Senior Clinical Trial Manager

Summary

The Senior Clinical Trial Manager is responsible for managing all operational aspects of clinical studies from setup to final report. They implement eTMF systems, develop SOPs, manage budgets, and interact with investigators and sites. The candidate must have a BS/BA degree in a scientific discipline, advanced degree preferred, and at least 5 years of experience in a biotech/pharmaceutical company or related healthcare industry.

Requirements

• BS/BA degree in a scientific discipline; advanced degree preferred
• Minimum of 5+ years demonstrated experience in a biotech/pharmaceutical/ CRO company, clinical research site or related healthcare company
• Experience with eTMF implementation and management of eTMF vendor
• Understanding of inspection readiness task and participation in inspection activities
• Prior experience with a multi-phase clinical program or experience across multiple phases of clinical drug development
• Highly organized, outcome oriented, self-motivated performance
• Thrives in a fast-paced and evolving environment
• Excellent interpersonal skills, ability to develop important relationships with key stakeholders across a variety of disciplines, good conflict management and negotiation skills
• Ability to analyze complex issues to develop relevant and realistic plans, programs, and recommendations
• Understanding of the drug development process
• Knowledge of federal regulatory requirements and guidelines for Good Clinical Practice
• Strong written and oral communication skills

Responsibilities

• Implementation of eTMF vendor (Veeva) and development of eTMF SOPs
• Review of eTMF documents both internal and at study CRO
• Implement clinical project plans in accordance with key study documents and corporate and regulatory objectives
• Facilitate internal project team meetings
• Drive all aspects of study start-up, including CRO selection
• Point of contact for sites, vendors and CROs
• Monitor CRO and vendor adherence to scope of work
• Manage interactions with investigators and investigative sites to ensure activities are conducted in accordance with all regulatory requirements
• Proactively identify, resolve, and escalate issues that jeopardize timely clinical study completion
• Develop and manage clinical trial budget and facilitate contract review
• Participate in vendor, site and CRO audits as appropriate
• Participate in site monitoring visits as necessary
• Plan and present at Investigator Meetings, company, and other meetings as necessary
• Develop internal tracking and reporting tools for reporting study status to Leadership
• Adhere to all department SOPs, GCP/ICH guidelines, and QC/QA procedures