Source Job

  • Manage global, multi-center clinical research projects in various therapeutic areas.
  • Deliver projects on time, within budget, and to high quality standards while leading multifunctional teams.
  • Serve as primary client contact, participate in bid defenses, and ensure compliance with procedures.

Clinical Research Project Management Team Leadership Communication Negotiation

15 jobs similar to Clinical Lead Project Manager

Jobs ranked by similarity.

US

  • Lead and manage a team of Project Directors and Project Managers for global clinical trials.
  • Oversee project delivery, sponsor interactions, and profitability across clinical programs.
  • Ensure compliance with GCP/ICH and drive continuous improvement and KPIs.

Precision Medicine Group is a precision medicine company providing clinical research and development services. They emphasize quality, people, clients, and performance, with a collaborative team environment.

$128,000–$182,000/yr
US Unlimited PTO

  • Lead all clinical study operations, providing strategic planning and direction from inception through completion.
  • Serve as the primary contact with sponsors and oversee study budgets, timelines, and vendor management.
  • Mentor and motivate study team members while ensuring compliance with GCP, protocols, and regulatory requirements.

ProTrials is a women-owned, WBENC-certified Contract Research Organization (CRO) that has been a trusted partner in clinical research since 1996. Our team of skilled professionals is committed to advancing clinical research with care, integrity, and excellence, fostering a collaborative and supportive culture.

Global

  • Provide leadership and mentorship across regional clinical trials while ensuring high-quality study execution with minimal travel.
  • Oversee monitoring visit reports, manage study risks, and ensure compliance with corrective measures at country and regional levels.
  • Collaborate with cross-functional teams, lead project calls, and deliver training to support data integrity and site performance.

PSI CRO is a privately owned, global Contract Research Organization dedicated to advancing medical science and bringing new therapies to patients worldwide. Founded in 1995, the company has over 3,000 employees and prides itself on long-term stability, having never undergone a merger, acquisition, or company-wide layoffs.

UK Hungary Poland Romania Serbia Slovakia

  • Manage clinical elements of trials including site selection, start-up, enrollment, monitoring, and close-out for studies across multiple countries.
  • Lead CRAs and ensure timeline adherence, quality delivery, and effective communication with cross-functional teams and sponsors.
  • Identify risks to project timelines, create action plans, and mentor team members while maintaining focus on study priorities.

Precision for Medicine is a precision medicine CRO that combines novel clinical trial designs, biomarker and data analytics, with a focus on rare diseases and oncology. The company is part of Precision Medicine Group, a growing organization dedicated to advancing oncology development and positively impacting patient health.

Slovakia

  • Provide operational leadership and oversight for assigned FSP projects, managing regional trials or supporting complex global trials.
  • Serve as the primary operational point of contact for clients, coordinating cross-functional activities and monitoring project risks, resource constraints, and quality trends.
  • Contribute to financial oversight, meeting facilitation, and team onboarding, training, and mentoring.

Precision Medicine Group is a clinical research organization (CRO) focused on supporting clients researching ground-breaking cancer therapies. The company fosters a supportive, collaborative environment that promotes work-life balance and team development.

$142,400–$224,100/yr
US

  • Manage a team of 6-14 CRAs to ensure excellent study and site performance with strict adherence to local regulations, company SOPs, and ICH GCP.
  • Provide training, support, and mentoring to CRAs, manage low or non-performance situations, and contribute to capacity planning.
  • Collaborate with local stakeholders, including CRMs and PLMs, to ensure alignment across monitoring functions and resolve site or CRA operational issues.

We are a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare, supported by a large and diverse workforce.

US

  • Manage execution of study-level activities, including creating trial documents and overseeing vendor delivery and budgets.
  • Coordinate country and regional trial management, aligning feasibility strategies and mitigating local risks.
  • Support program-level compound training and mentor new team members in Trial Management.

Johnson & Johnson is a global healthcare innovator focused on preventing, treating, and curing complex diseases through Innovative Medicine and MedTech. With a large workforce, they emphasize an inclusive work environment guided by their Credo, respecting diversity and dignity.

Europe

  • Leads new and existing CRO laboratory projects, ensuring project plans are translated into action and results.
  • Manages all aspects of designated protocols, accountable for overall project performance and client satisfaction.
  • Provides internal consulting on project management issues and identifies opportunities for process improvement.

Precision for Medicine is a contract research organization that accelerates the development of novel therapeutics through laboratory services. The company fosters a collaborative culture and is dedicated to advancing clinical research globally.

US

  • Leads the planning, conduct, and oversight of clinical studies per scope of work, ensuring compliance with protocols, SOPs, and regulatory requirements.
  • Acts as primary clinical point of contact for clients, develops study documents, and drives site feasibility and recruitment strategies.
  • Manages clinical teams, training, vendor oversight, and ensures data quality and timely deliverables across study phases.

Precision Medicine Group is a clinical research organization that provides outsourced clinical trial management services to pharmaceutical and biotechnology companies. The company fosters a collaborative culture focused on quality and compliance, and employs a team of experienced clinical professionals.

US Unlimited PTO

  • Lead and maintain integrated project plans, drive cross-functional execution, and facilitate team meetings to ensure accountability and progress.
  • Proactively identify and manage risks, develop mitigation strategies, and support governance readiness with decision-focused materials.
  • Partner with cross-functional teams to improve planning, execution, and operational processes in a lean, fast-paced environment.

Definium Therapeutics is a late-stage clinical biopharmaceutical company developing psychedelic-based treatments for psychiatric disorders. The company is publicly traded on Nasdaq and fosters a culture of scientific rigor and innovation.

$85–$100/hr
United States

  • Manage cross-functional teams to execute pharmaceutical marketing campaigns on time and on budget.
  • Oversee account budgets, forecasts, and financial performance to optimize profitability.
  • Ensure compliance with medical, legal, and regulatory requirements in the US and Canada.

P10 is a pharmaceutical marketing agency that challenges traditional agency models with a focus on passion and purpose. They bring together a diverse team of remote-only seasoned professionals to deliver exceptional value for clients.

US

  • Lead and oversee global drug development programs, ensuring alignment with strategic objectives and key milestones.
  • Facilitate cross-functional collaboration by coordinating program meetings, tracking decisions, and managing risks.
  • Drive effective decision-making, support budget planning, and mentor stakeholders to enhance operational excellence.

Our partner is a biotechnology or pharmaceutical company advancing innovative therapies through the full drug development lifecycle. They foster a fast-paced, mission-driven environment with cross-functional global teams, focusing on oncology innovation and healthcare impact.

US

  • Lead site activation strategies and oversee start-up activities across clinical studies.
  • Manage critical path plans and mitigate risks to ensure timelines are met.
  • Collaborate with cross-functional teams and clients to improve activation processes.

Our partner is a clinical research organization that supports the delivery of clinical trials. They are a global company with a collaborative culture focused on innovation and operational excellence.

$125,000–$145,000/yr
US

  • Act as primary representative for eClinical Solutions and sponsor data management interaction, ensuring quality and timelines within scope.
  • Define specifications and collaborate with technical teams on configuration of elluminate for data cleaning strategy and oversight.
  • Perform quality oversight and data trending via elluminate reporting to identify risks and develop mitigation strategies.

eClinical Solutions helps life sciences organizations accelerate clinical development initiatives with expert data services and the elluminate Clinical Data Cloud. The company is a people-first organization with an inclusive culture, recognized as a 2025 Top Workplaces USA Award winner for Remote Work.

US Canada 4w PTO

  • Manage large multi-faceted projects and cross-functional teams in a pharmaceutical advertising agency setting
  • Act as communication hub between agency teams and partners, ensuring effective workflow and resource allocation
  • Develop timelines, manage budgets, and provide process improvements to enhance efficiency

Avalere Health is a healthcare advisory, medical, and marketing agency focused on reaching every patient possible. With offices globally and a strong emphasis on inclusive culture, they support employees through flexible working, parental leave, and professional development.