Associate Director – Senior Clinical Trial Manager II

Scholar Rock

. Implement clinical project plans in accordance with key study documents, corporate objectives, and regulatory objectives .

Posted 9/23/2026full-timeCambridge • Massachusetts • United StatesSenior💰 $155,000 - $225,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in managing clinical project plans, ensuring compliance with regulatory requirements, and facilitating effective communication among stakeholders. Proficient in budget management, vendor oversight, and adherence to Good Clinical Practice guidelines.

Highest-signal resume keywords

Clinical Project ManagementRegulatory ComplianceBudget Development and ManagementStakeholder CommunicationCRO and Vendor Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ManagementMulti-Phase Clinical Program ExperienceDrug Development Process KnowledgeGCP/ICH Guidelines UnderstandingContract Review

Soft Skills

Interpersonal SkillsConflict ManagementNegotiation SkillsOrganizational SkillsSelf-Motivated Performance

Tools & Technologies

Internal Tracking ToolsReporting Tools

Industry Keywords

BiotechPharmaceuticalCROClinical ResearchHealthcare

About the role

Key responsibilities & impact

Implement clinical project plans in accordance with key study documents, corporate objectives, and regulatory objectives
Facilitate internal project team meetings
Drive all aspects of study start-up, including CRO selection
Serve as point of contact for sites, vendors, and CROs
Monitor CRO and vendor adherence to scope of work
Manage investigator and investigative site interactions in accordance with regulatory requirements
Identify, resolve, and escalate issues jeopardizing timely clinical study completion
Develop and manage clinical trial budgets 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 meetings, and other meetings
Develop internal tracking and reporting tools for Leadership study-status reporting
Adhere to department SOPs, GCP/ICH guidelines, and QC/QA procedures
Travel internationally and domestically up to 20% as required
Perform other duties and responsibilities as required

Requirements

What you’ll need

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
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