Senior Director Clinical Project Management


Maryland
Permanent
USD250000 - USD275000
Clinical
PR/588115_1776125941
Senior Director Clinical Project Management

Director / Senior Director, Clinical Program Operations

Remote (United States)

$175,000 - $215,000 base salary

Job Description

We are partnered with a late-stage, clinically focused biotechnology organization that is advancing multiple therapeutic programs addressing areas of high unmet medical need. The company is expanding its clinical development leadership team and is seeking a Director / Senior Director, Clinical Program Operations to oversee the operational execution of complex global clinical studies.

This role offers the opportunity to lead programs with meaningful clinical impact while working crossfunctionally in a fastpaced, highly collaborative environment. The ideal candidate brings strong operational leadership, handson trial execution experience, and a track record of successfully managing CROs and external partners across study phases.

Key Qualifications

* Extensive experience leading clinical trial operations within the pharmaceutical or biotechnology industry, including oversight of global clinical studies.

* Demonstrated success managing CROs, vendors, and external partners, ensuring delivery against timelines, budgets, and quality expectations.

* Strong understanding of ICHGCP, FDA, EMA, and other applicable global regulatory requirements.

* Proven ability to manage complex operational challenges related to patient enrollment, site performance, and protocol execution.

* Experience in metabolic disease or MASH highly preferred

* Experience developing and maintaining essential clinical documentation, including protocols, monitoring strategies, and operational plans.

* Ability to assess operational risks and implement proactive mitigation strategies across clinical programs.

* Excellent communication and leadership skills, with the ability to influence crossfunctional teams and executive stakeholders.

Roles & Responsibilities

* Lead the endtoend operational execution of assigned clinical studies, from study startup through closeout.

* Serve as the primary operational liaison with CROs and thirdparty vendors, ensuring adherence to scope, timelines, and quality standards.

* Provide handson oversight of daytoday clinical operations activities, maintaining alignment with program goals and development strategy.

* Collaborate with internal functions including clinical development, regulatory, data management, safety, and quality to ensure seamless study execution.

* Oversee Trial Master File (TMF) strategy, ensuring inspection readiness and compliance throughout the study lifecycle.

* Identify, escalate, and resolve operational risks affecting enrollment, site performance, or data quality.

* Support continuous improvement initiatives within clinical operations, driving process efficiency and best practices.

* Contribute to strategic planning discussions related to future clinical programs and operational infrastructure.

Benefits

* Comprehensive medical, dental, and vision coverage

* 401(k) with company contribution

* Competitive PTO and paid holidays

FAQs

Congratulations, we understand that taking the time to apply is a big step. When you apply, your details go directly to the consultant who is sourcing talent. Due to demand, we may not get back to all applicants that have applied. However, we always keep your resume and details on file so when we see similar roles or see skillsets that drive growth in organizations, we will always reach out to discuss opportunities.

Yes. Even if this role isn’t a perfect match, applying allows us to understand your expertise and ambitions, ensuring you're on our radar for the right opportunity when it arises.

We also work in several ways, firstly we advertise our roles available on our site, however, often due to confidentiality we may not post all. We also work with clients who are more focused on skills and understanding what is required to future-proof their business. 

That's why we recommend registering your resume so you can be considered for roles that have yet to be created. 

Yes, we help with CV and interview preparation. From customized support on how to optimize your CV to interview preparation and compensation negotiations, we advocate for you throughout your next career move.

Handpicked roles for you