Senior Clinical Project Manager

Deciphera Pharmaceuticals

. Lead the planning, execution, and delivery of assigned global clinical studies .

Posted 11/5/2026full-timeRemote • Massachusetts • United StatesSenior💰 $138,000 - $168,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive experience in managing global clinical studies, with a strong focus on Phase II and III trials. Proficient in leading cross-functional teams, managing CROs, and ensuring compliance with GCP, ICH, and FDA regulations.

Highest-signal resume keywords

Global Clinical Trial ManagementCross-Functional Team LeadershipCRO ManagementGCP, ICH, FDA KnowledgeClinical Study Budget Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Research ExperiencePhase III Study ManagementOperational Risk ManagementClinical Trial ExecutionBudget Management

Soft Skills

Strong Communication SkillsProblem-Solving SkillsIndependent Work AbilityAdvocacy Skills

Tools & Technologies

ETMFEDCIWRSRBQM Platforms

Certifications & Qualifications

PMP Certification

Industry Keywords

Oncology Clinical DevelopmentRare Disease Clinical DevelopmentBiotechnology EnvironmentClinical Operations

Tech Stack

Tools & technologies

Google Cloud PlatformPMP

About the role

Key responsibilities & impact

Lead the planning, execution, and delivery of assigned global clinical studies
Manage study timelines, budgets, quality, and overall operational execution
Identify and address operational risks and challenges to keep studies on track
Lead cross-functional study teams, driving collaboration, accountability, decision-making, and problem-solving
Partner with Clinical Operations, Data Management, Regulatory, Clinical Supply, and other functions
Oversee CROs and external vendors
Monitor CRO and vendor performance and ensure alignment with timelines, budgets, quality expectations, and contractual obligations
Communicate study progress, risks, and key decisions to internal stakeholders and Clinical Operations leadership
Contribute to Clinical Operations processes and ways of working that support efficient, high-quality study execution
Perform other duties and responsibilities as assigned

Requirements

What you’ll need

Bachelor’s degree in health science or a related field
8+ years of clinical research experience, including meaningful responsibility for managing complex clinical trials
Strong global clinical trial and later-stage development experience, ideally including Phase III
Substantial experience leading large, complex Phase II studies will also be considered
Demonstrated ability to lead and influence cross-functional study teams
Hands-on experience managing CROs and vendors and proactively addressing operational risks
Strong working knowledge of GCP, ICH, FDA, and applicable global clinical trial requirements
Strong communication and problem-solving skills
Ability to work independently, advocate for what is needed, and recognize when to engage others for support
Preferred: Phase III global study experience
Preferred: Oncology or rare disease clinical development experience
Preferred: Experience with eTMF, EDC, IWRS, and RBQM platforms
Preferred: Experience managing clinical study budgets and contracts
Preferred: Experience within a fast-paced biotechnology environment
Preferred: PMP certification or equivalent project management training
Availability for occasional early-morning or evening meetings across time zones
Travel of approximately 25% may be required, including travel to Boston approximately twice per year and attendance at relevant conferences or study-related meetings

Benefits

Comp & perks

Competitive salary and annual bonus
Long-term incentive plan
Full range of benefits and other incentive compensation plans (if applicable)
Medical, dental, and vision insurance
401(k) retirement plan with company match
Generous parental leave
Family planning benefits
Opportunities for personal and professional growth