Source Job

Global

  • Lead the planning, execution, and management of clinical trials.
  • Ensure compliance with FDA, ICH-GCP, and other regulatory standards.
  • Supervise and mentor Clinical Research Associates (CRAs) and study coordinators.

Clinical Research Project Management Leadership

20 jobs similar to Sr. Clinical Research Manager

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US

  • Ensure departmental compliance with all applicable global regulations and Sarah Cannon SOPs.
  • Establish and lead the clinical operations strategy, setting departmental goals.
  • Promote strong cross‑functional collaboration with internal stakeholders.

McKesson delivers products to healthcare providers. Every day, McKesson’s employees deliver products to healthcare providers that make a difference in the care and life of a patient, focused on creating an inclusive environment with strong values.

US

  • Assist with daily site activities, acting as the primary point of contact for the site.
  • Assist with training and mentoring research staff, upholding professional development goals.
  • Promote strict adherence to ICH-GCP, FDA, and local regulations, maintaining audit readiness across all studies.

Care Access aims to improve the future of health for everyone. They operate globally with research locations, mobile clinics, and clinicians, bringing health services to communities, and are dedicated to ensuring every person can understand their health, access care, and contribute to medical progress.

Europe

  • Oversee clinical budgets and develop monitoring plans for effective study oversight.
  • Train and mentor Clinical Research Associates (CRAs) to optimize their performance.
  • Drive enrollment and lead study start-up activities, adhering to timelines.

Jobgether employs AI to match candidates to job openings, ensuring fair and objective reviews. They connect top candidates with hiring companies, who then manage the final decisions and interview process.

Europe

  • Management and operational delivery of the clinical elements within a trial.
  • Successful execution of assigned trials and ensuring completion of trial deliverables.
  • Identify challenges to study timelines/deliverables and offer creative action plans.

Precision for Medicine is a precision medicine CRO with a uniquely integrated offering to enable the science of precision medicine. They achieve this by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions. They are dedicated to positively impacting the health and lives of patients around the world, particularly in rare diseases and oncology.

Global

  • Manage a portfolio of sponsor and client accounts, leading recurring calls, business reviews, and ad-hoc engagements.
  • Drive responsiveness and service levels for sponsor requests, communicating with accuracy and awareness of business risks.
  • Translate sponsor goals into cross-functional delivery plans.

Jobgether is a company that uses an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. They identify the top-fitting candidates, and this shortlist is then shared directly with the hiring company.

$90,000–$133,000/yr

  • Monitor clinical studies of investigational and approved products.
  • Manage and train site personnel on therapeutic area, protocol requirements, proper source documentation, and case report form completion.
  • Review data queries and listings, and work with the study centers to resolve data discrepancies.

ProTrials is a women-owned, WBENC-certified Contract Research Organization (CRO) that has been a trusted partner in clinical research since 1996. They believe great work happens when team members feel valued, supported, and empowered, and they are committed to making a meaningful impact on global health.

US Unlimited PTO

  • Directs the operational oversight and execution of clinical site start-up.
  • Manages CRO relationship and oversight to ensure appropriate scope of work.
  • Develops collaborative relationships with investigative sites.

Bristol Myers Squibb is focused on developing innovative drugs against targets of solid tumors. They are a dynamic biotechnology company headquartered in San Diego, CA, and aim to be the global leader in radiopharmaceuticals.

US

  • Directly manage a remote team of Care Partners, providing guidance and support.
  • Design and improve operational processes to ensure high clinical quality.
  • Monitor key performance indicators to measure success across different teams.

Medsien provides scalable remote care management for a quality patient experience. Hundreds of organizations trust Medsien's technology solutions to implement remote care management programs, personalize every interaction, and improve the lives of the people who need it most.

US Canada

  • Collaborate with dedicated research sites contributing to rare neurological disease research.
  • Make a significant impact in the scientific community alongside a dedicated team of CRAs.
  • Encompass important site monitoring and management activities including SIVs Interim and Remote Monitoring Visits as well as Final Onsite and Closeout Visits.

St. Joseph's Hospital and Medical Center is a 571-bed, not-for-profit hospital providing health, social, and support services. They are dedicated to caring for the poor and underserved, and are known for quality quaternary care, medical education, and research.

$100,000–$150,000/yr
US

  • End-to-end management of the clinical trial agreement (CTA) process for global, multi-site clinical trials.
  • Develop the study-specific CTA strategy with the Sponsor and internal stakeholders.
  • Negotiate CTAs and the corresponding budget directly with clinical sites.

Jobgether uses an AI-powered matching process to ensure applications are reviewed quickly, objectively, and fairly. Their system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company.

Europe

  • Provides regulatory guidance throughout the clinical development life cycle
  • Compile, coordinate and review applications to Regulatory Authorities
  • Develops and/or reviews documents intended for submission to the Regulatory Authorities and/or Ethics Committees

Precision for Medicine integrates clinical trial execution with scientific knowledge, lab expertise, and data science to improve the speed, cost, and success rate of life-changing therapies. They focus on Oncology and Rare Disease and value employee contributions.

Singapore

  • Serve as primary point-of-contact and primary escalation point to the client.
  • Coordinate and oversees all functional services including external vendors to the established timeline and budget.
  • Develop robust and comprehensive project plans, including timelines and proactive risk management and mitigation, to guide all parameters of trial execution with consistency and quality.

Precision for Medicine integrates clinical trial execution with scientific knowledge, laboratory expertise, and advanced data sciences to improve the speed, cost, and success rate of bringing therapies to patients. They focus on Oncology and Rare Disease and strive to ensure employees feel appreciated and valued for their contributions every day.

$130,000–$140,000/yr
US

  • Collaborate with stakeholders to execute clinical strategies that align with business objectives.
  • Drive the performance of clinical support employees, ensuring exceptional patient care and technical expertise.
  • Lead efforts to improve healthcare access and equity with compassion and purpose.

Jobgether uses an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Their system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company.

US

  • Lead and develop a team of RN Care Coordinators and non-clinical Care Coordinators.
  • Ensure timely progression of members through the surgical review and COE pathways.
  • Identify workflow issues and recommend process improvements.

Transcarent and Accolade have come together to create the One Place for Health and Care, the leading personalized health and care experience that delivers unmatched choice, quality, and outcomes. Together, more than 20 million people have access to the combined company’s offerings.

Europe

  • Manage a portfolio of accounts, leading recurring calls and business reviews.
  • Translate sponsor goals into cross-functional delivery plans.
  • Collaborate with Clinical Operations to improve sponsor experience.

Jobgether is a platform that uses AI-powered matching process to ensure applications are reviewed quickly, objectively, and fairly. They use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements.

US

  • Oversight for traveling clinical staff supporting decentralized operations at events and sites.
  • Ensure high-quality protocol execution, participant safety, and adherence to GCP and FDA regulations.
  • Manage, develop, and evaluate all clinical research staff (CRCs, nurses, mobile clinicians, and traveling staff).

Care Access aims to improve the future of health for everyone. With numerous research locations and clinicians globally, they deliver research and health services to communities facing barriers to care.

US 3w PTO

  • Ensure adherence to regulations and contractual obligations.
  • Develop and update compliance policies and SOPs.
  • Conduct internal compliance audits and report findings.

Equip is a virtual, evidence-based eating disorder treatment program. They aim to ensure that everyone with an eating disorder can access effective treatment, operating in all 50 states and partnered with most major health insurance plans. Since its founding in 2019, Equip has maintained a fully virtual environment.

$119,000–$148,700/yr
US

  • Manage and drive continuous process improvement initiatives.
  • Oversee all daily, end to end, clinical trial/patient matching operations.
  • Serve as a liaison between trial sites, sponsors, and drive project delivery.

Natera is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for their work and each other.

$100,000–$170,000/yr
US

  • Assist with the development of the protocol and informed consent form and/or program design.
  • Manage vendor budgets, payments, and timelines.
  • Effectively track and report on internal project metrics and study progress.

Tonix is a fully integrated biotechnology company, publicly traded on NASDAQ (ticker: TNXP), with marketed products and a pipeline of development candidates. They are focused on commercializing, developing, discovering, and licensing therapeutics to treat and prevent human disease and operates a state-of-the art infectious disease research facility. They provide a comprehensive compensation and benefits package.

$111,200–$198,650/yr
US

  • Provide leadership and guidance to multiple sales representatives on the Compliance Sales Team.
  • Develop and oversee the execution of advanced sales strategies that align with organizational objectives.
  • Drive significant revenue growth through innovative sales initiatives and market expansion.

Wolters Kluwer provides expert software and information solutions that the world’s leading professionals rely on, in the moments that matter most. The group serves customers in over 180 countries, maintains operations in over 40 countries, and employs approximately 21,400 people worldwide.