Sr. Clinical Study Manager

Clinical Project Leader

The Clinical Project Leader serves as a senior clinical trial operations leader responsible for overseeing large, complex Phase II, III, and IV clinical research studies from startup through closeout. This role acts as the primary operational point of contact, ensuring studies remain on schedule, within scope, and compliant with regulatory and protocol requirements. The position focuses heavily on large global cardiovascular and metabolic trials, including diabetes, obesity, and heart disease, and requires extensive collaboration with sponsors, investigators, vendors, and cross-functional internal teams. The Clinical Project Leader provides strategic oversight of site startup, trial execution, risk management, and stakeholder communication while serving as the operational face of the trial to clients and external partners. Responsibilities

- Lead the day-to-day operations of Phase II, III, and IV clinical trials from study startup through closeout.
- Ensure clinical studies remain on schedule, within scope, and compliant with protocol, Good Clinical Practice (GCP), and applicable regulatory requirements.
- Coordinate and align activities between sponsors, sites, investigators, vendors, and internal cross-functional teams.
- Identify operational risks, troubleshoot issues, and develop practical solutions to keep projects on track.
- Drive study startup activities, including site activation, regulatory submissions, essential document collection, and investigator readiness.
- Ensure sites are fully prepared to begin enrollment and conduct study procedures according to protocol and regulatory standards.
- Oversee trial progress after startup, maintaining operational oversight and performance monitoring through study completion.
- Serve as a primary client-facing contact for sponsors and key study stakeholders throughout the project lifecycle.
- Lead study meetings and present clear updates on timelines, enrollment status, risks, and key project milestones.
- Build and maintain strong relationships with sponsors, investigators, site personnel, vendors, and internal teams.
- Communicate effectively and professionally with internal and external partners, managing expectations and ensuring alignment.
- Provide guidance, mentorship, and support to junior Project Leaders and study team members.
- Lead cross-functional meetings, ensuring all stakeholders understand priorities, responsibilities, and project objectives.
- Contribute to the development and refinement of study processes, workflows, and operational best practices.
- Monitor study performance and compliance, addressing operational or quality concerns in a timely and proactive manner.
- Support protocol amendments, process improvements, and change management activities as needed.
- Ensure adherence to GCP, FDA regulations, and institutional policies across all trial activities.
- Manage complex operational logistics associated with multi-country, multi-site global trials.
- Oversee and track site startup timelines and milestones, ensuring timely site activation and enrollment readiness.

Essential Skills

- At least 7+ years of experience in a Clinical Project Leader III or equivalent senior clinical project leadership role within a contract research organization (CRO).
- Bachelors degree (4-year degree) in a relevant field or equivalent education and experience.
- Significant clinical trial management experience overseeing complex, multi-site studies.
- Proven experience leading Phase II, III, and/or IV clinical trials.
- Strong understanding of clinical operations, study conduct, and regulatory requirements, including GCP and FDA regulations.
- Demonstrated experience working across multiple functional groups and stakeholders in a matrix environment.
- Extensive experience managing large global trials involving multiple countries, international study teams, and global investigators and sites.
- Background in cardiovascular and/or metabolic disease clinical research, including areas such as diabetes, obesity, and heart disease.
- Expertise in site startup and study activation, including site activation processes, regulatory submissions, essential document collection, and site readiness

Additional Skills & Qualifications

- Experience leading large global Phase II/III trials within a CRO environment.
- senior Clinical Project Leader Background, ideally at the PL III level.
- Strong cardiovascular and metabolic therapeutic area expertise, including experience with diabetes, obesity, and heart disease trials.
- Demonstrated ability to serve as the operational face of the trial to sponsors and external partners.
- Experience developing and refining study processes, workflows, and operational best practices.
- Strong communication, negotiation, and conflict-resolution skills with the ability to escalate and resolve issues professionally.
- Proven ability to work independently while contributing to a collaborative team culture.
- Preference for candidates located in or able to work effectively within the Eastern Time Zone.
- Comfort working in a fast-paced, mission-driven environment with high expectations for quality and performance.
- Motivated, go-getter mindset with a willingness to go the extra mile to support the team and project success.

Work Environment This role offers a 100% remote work environment with a remote-friendly structure that supports flexibility and work-life balance. The position is well-suited for candidates who can work effectively within the Eastern Time Zone, as collaboration with sponsors, investigators, and internal teams may align with that schedule. The work involves extensive use of clinical trial technology platforms and trial management systems to support trial management, site activation, regulatory tracking, clinical operations oversight, and study reporting. You will operate within a mission-driven, collaborative culture that values transparency, inclusion, shared success, and high-quality execution. The environment is fast-paced and high-visibility, providing opportunities to contribute to impactful clinical research while benefiting from training, mentorship, and exposure to diverse therapeutic areas.
Job Type & Location
This is a Contract position based out of Princeton, NJ.
Pay and Benefits
The pay range for this position is $80.00 - $90.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors. Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:

Medical, dental & vision
Critical Illness, Accident, and Hospital
401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
Life Insurance (Voluntary Life & AD&D for the employee and dependents)
Short and long-term disability
Health Spending Account (HSA)
Transportation benefits
Employee Assistance Program
Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully remote position.
Application Deadline
This position is anticipated to close on Oct 16, 2026. About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.

If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email [email protected] for other accommodation options.

San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.

Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
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shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
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