Clinical Trial Managers oversee the planning and execution of clinical studies, helping ensure trials meet scientific, operational, regulatory, and ethical requirements. They coordinate cross-functional teams, manage timelines and budgets, and monitor progress from study startup through closeout. Explore vetted Clinical Trial Manager opportunities with compensation of $100,000 or more on Ladders.
Responsibilities vary by employer and study, but commonly include developing trial plans, coordinating clinical research organizations and sites, tracking enrollment and milestones, managing study budgets, and identifying operational risks. Clinical Trial Managers also support compliance with protocols, Good Clinical Practice (GCP), and applicable regulatory requirements, while communicating updates to sponsors, investigators, and internal stakeholders.
Employers often seek experience in clinical research or trial operations, strong project management and communication skills, and the ability to manage multiple priorities. Familiarity with GCP, clinical trial regulations, study documentation, and systems such as electronic data capture platforms can be valuable. A degree in life sciences, nursing, public health, or a related field is common; some positions may prefer advanced education or relevant certifications.
Clinical Trial Managers work for pharmaceutical and biotechnology companies, contract research organizations, academic medical centers, and other research organizations. Opportunities may focus on a therapeutic area, phase of development, or regional portfolio. With experience, professionals may advance to senior trial management, clinical operations leadership, or program management roles.
Search Ladders for Clinical Trial Manager jobs and related clinical operations opportunities. Compare roles by responsibilities, experience requirements, work arrangement, and compensation to find positions that align with your career goals.
Associate Director, Medical Writing - Clinical & Regulatory
$120K - $145K *
Drive the development of high-quality regulatory documents for clinical trials and submissions, collaborating with cross-functional teams to ensure compliance with global health authority standards in...
1 week ago
Associate Director, Medical Writing - Clinical & Regulatory
$120K - $145K *
Elevate your career by leading regulatory document development for clinical trials and submissions. Collaborate with cross-functional teams to ensure compliance with global health authority standards...
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Transform quality assurance by leading batch disposition and compliance efforts. Drive cross-functional collaboration to enhance operational effectiveness and ensure timely release of drug substances...
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Senior Clinical Research Coordinator - Gurnee, IL
$80K - $95K *
Join a dynamic team as you lead complex clinical trials, mentor staff, and enhance patient experiences while ensuring compliance and operational excellence in a fast-paced research environment...
1 week ago
Patient and Site Engagement Lead (US/UK)
$90K - $178K *
Transform the patient engagement landscape in clinical trials by developing and delivering strategic support initiatives. Partner with diverse stakeholders to enhance participation and optimize patien...
Reposted 1 week ago
Sr. Mngr/Associate Director, Process Design & Deployment
$110K - $130K *
Join our team to enhance patient access and streamline operational processes, driving meaningful improvements through data analysis, project management, and collaboration across departments while fost...
Reposted 4 weeks ago
Associate Director/Director Project Management
$135K - $160K *
Champion cross-functional project management for drug development, ensuring effective planning, execution, and governance across complex initiatives. Collaborate with diverse teams to drive Phase 3 re...
1 week ago
Associate Director/Director Project Management
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Join a dynamic team to drive strategic project management for drug development, ensuring effective execution and collaboration across functions while navigating complex regulatory landscapes and prepa...
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Drive impactful technology projects by collaborating with stakeholders to ensure seamless execution and alignment across diverse teams. Leverage your expertise in project management to navigate comple...
3 days ago
Quality Operations Manager (Contract)
$100K - $120K *
Contribute to quality operations initiatives by reviewing study documents, supporting audits, and ensuring compliance with regulatory standards. Collaborate with cross-functional teams to enhance qual...
6 days ago
Clinical Research Associate II - Oncology (Central Tennessee)
$80K - $95K *
Engage with clinical sites to enhance trial performance and data integrity. Collaborate with investigators and staff to ensure compliance and improve patient recruitment, while mentoring junior team m...
2 days ago
Senior Clinical Research Associate-- CNS/ - Psychiatry - Southeast
$97K - $193K *
Join a team that's dedicated to advancing clinical research by managing site activities throughout the study lifecycle, ensuring high-quality trial delivery, and supporting patient safety in a collabo...
1 week ago
Senior Budget Administrator - Clinical Trials
$100K - $161K *
Advance your career by coordinating clinical trial budgets and coverage analyses. Collaborate with stakeholders to ensure compliance and cost efficiency while mentoring junior staff and enhancing admi...
1 week ago
$120K - $145K *
Empower a dynamic team to design and implement full stack software solutions, balancing hands-on engineering with leadership. Drive innovation in web applications using modern technologies while foste...
1 week ago
$110K - $130K *
Champion successful implementations by leveraging scientific expertise and project management skills to transform R&D processes for diverse biotech and pharma clients, ensuring high-quality deployment...
Yesterday
$125K - $135K *
Transform project execution in regulated environments by managing scope, schedule, and resources for facilities and engineering projects. Collaborate with cross-functional teams to ensure compliance a...
2 days ago
$88K - $105K *
Advance your career by managing strategic client projects, ensuring seamless delivery and collaboration. Shape client strategies and improve processes while contributing to global healthcare initiativ...
2 weeks ago
Regional Manager, Device Support Specialist
$92K - $130K *
Transform patient support by leading a dedicated field team, ensuring high-quality service and operational excellence across the Midwest. Drive performance improvements and foster team development whi...
Yesterday
$120K - $181K *
Lead regulatory strategies to ensure global product compliance and approval. Collaborate with cross-functional teams to drive successful submissions and maintain regulatory standards, while fostering...
1 week ago
$120K - $181K *
Manage regulatory strategies for global product approvals, ensuring compliance and collaboration across teams. Lead submission activities for medical devices, fostering a high-performance culture whil...
1 week ago
Senior Manager, Global Site Start-Up Lead
$134K - $219K *
Unlock potential by leading global site start-up strategies for complex clinical trials. Drive operational excellence, ensure compliance, and collaborate with cross-functional teams to accelerate stud...
Reposted 2 weeks ago
Manager, CMC Regulatory Affairs - Biologics
$108K - $176K *
Elevate progress at the forefront of CMC Regulatory Affairs, leading strategies and compliance for biologics. Collaborate with global teams to ensure regulatory excellence throughout development and p...
2 weeks ago
Manager, CMC Regulatory Affairs - Biologics
$108K - $176K *
Accelerate progress at the forefront of CMC Regulatory Affairs, leading strategies and compliance for biologics. Collaborate with global teams to ensure regulatory excellence throughout product develo...
2 weeks ago
Manager, CMC Regulatory Affairs - Biologics
$108K - $176K *
Elevate your career by leading regulatory strategy and compliance for biologic products. Collaborate with cross-functional teams to ensure adherence to global regulations and drive efficiency in CMC p...
2 weeks ago
Manager, CMC Regulatory Affairs - Biologics
$108K - $176K *
Champion CMC regulatory strategies for biologics, ensuring compliance and efficiency in submissions, interactions, and process improvements while leading cross-functional teams to navigate complex reg...
2 weeks ago
What does a Clinical Trial Manager do?
A Clinical Trial Manager plans and coordinates clinical studies, overseeing timelines, budgets, vendors, research sites, study teams, and operational compliance from startup through closeout.
What qualifications are typically required for Clinical Trial Manager jobs?
Many roles require clinical research or trial operations experience, project management skills, and knowledge of GCP and relevant regulations. Employers commonly seek a degree in life sciences, nursing, public health, or a related area.
Where do Clinical Trial Managers work?
They work at pharmaceutical and biotechnology companies, contract research organizations, academic medical centers, and other organizations that sponsor or conduct clinical research.
How can I find Clinical Trial Manager jobs paying $100,000 or more?
Browse vetted Clinical Trial Manager openings on Ladders, where listed opportunities pay $100,000 or more. Review each posting for compensation details, qualifications, and work arrangement.