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.
Senior Statistical Programmer FSP
$110K - $130K *
Lead advanced SAS programming efforts to support Phase I-IV clinical trials, ensuring data integrity and compliance with CDISC standards. Collaborate with cross-functional teams to deliver high-qualit...
4 weeks ago
Senior Director, Clinical Quality Assurance (CQA)
$245K - $286K *
Elevate clinical quality assurance through strategic leadership and oversight of global trials, ensuring compliance with GCP regulations. Drive quality culture and inspection readiness while mentoring...
Reposted 3 weeks ago
Medical Affairs and Evidence Generation Asset Lead – Executive Director
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Elevate medical affairs by providing strategic insights for clinical asset development and commercialization. Lead cross-functional teams, execute evidence generation plans, and foster collaboration t...
Reposted 1 week ago
Director, Head of Patient Recruitment and Retention, Americas
$171K - $231K *
Drive innovative patient recruitment strategies to enhance clinical trial enrollment and retention. Collaborate with cross-functional teams to implement data-driven approaches, optimize patient engage...
Reposted 4 weeks ago
Global Study Management Associate
$72K - $97K *
Join a dynamic team to support global clinical study delivery, ensuring quality and compliance in clinical operations. Collaborate with cross-functional teams to manage study logistics, data tracking...
Yesterday
$115K - $127K *
Join a team that's dedicated to advancing oncology research by monitoring clinical trials, ensuring compliance, and supporting investigative sites throughout the trial lifecycle. Your expertise will d...
Yesterday
Regulatory Affairs Consultant, CMC - Biologics
$110K - $130K *
Drive your career with a pivotal role in CMC regulatory affairs, ensuring compliance for biologics and small molecules. Collaborate across teams to prepare high-quality submissions and strategies, imp...
2 days ago
Senior Technical Program Manager
$115K - $172K *
Shape the future of healthcare by leading complex data ingestion initiatives. Collaborate with cross-functional teams to drive program delivery, manage risks, and ensure operational excellence while t...
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Executive Director, Global Medical Affairs
$175K - $210K *
Elevate Global Medical Affairs by leading strategic initiatives and operational excellence. Drive innovation and scalable solutions while managing a high-performing team to enhance client value across...
Reposted today
$110K - $130K *
Join us to design and oversee the quality assurance framework for our AI platform. You'll implement automated testing, ensure compliance, and collaborate with cross-functional teams to maintain high-q...
3 weeks ago
Clinical Research Associate - Full-Service
$80K - $95K *
Engage in vital oversight of clinical research, ensuring compliance and data integrity through monitoring. Collaborate with site teams to enhance study quality, using innovative techniques to tackle c...
Reposted 2 days ago
Senior Director, National Field Excellence
$217K - $271K *
Launch your career by owning the national Field Excellence model, managing operations for a groundbreaking oncology therapy. Collaborate with sales leaders to enhance prescriber access and streamline...
1 week ago
Director, Clinical Pharmacology
$189K - $246K *
Lead clinical pharmacology strategies, integrating PK/PD assessments across development phases. Collaborate with cross-functional teams to guide decision-making and regulatory submissions, ensuring al...
Yesterday
Clinical Supply Chain Site Lead
$110K - $130K *
Champion the clinical supply chain for late-stage oncology trials, ensuring seamless operations and communication between sites, suppliers, and stakeholders. Drive continuous improvement and complianc...
1 week ago
Clinical Program Lead (CPL) - RLT Focus
$248K - $461K *
Grow your career with us by providing strategic medical leadership for oncology agent development, coordinating clinical strategies, guiding trials, and collaborating with international experts to dri...
Reposted 2 weeks ago
Sr. CRA - Phase 1 Oncology Southeast
$100K - $120K *
Empower clinical excellence by leading trial monitoring efforts, ensuring compliance with protocols and regulations. Collaborate with teams to enhance data integrity and site performance while guiding...
3 weeks ago
Principal IT Analyst - Veeva RIM
$121K - $161K *
Transform your career by leading the design and implementation of Veeva Vault RIM, ensuring optimal performance and compliance while collaborating with cross-functional teams to enhance user experienc...
3 weeks ago
Sr Editor, Consent Form Development
$66K - $116K *
Elevate your career by joining a team that reviews and edits informed consent forms, ensuring compliance with regulatory standards while mentoring new editors and enhancing organizational knowledge in...
1 week ago
Project Design Manager - Client Services
$88K - $105K *
Unlock potential by managing clinical trial project setups and amendments. Collaborate with teams to ensure client requirements are met, while serving as a subject matter expert to enhance process eff...
1 week ago
Clinical Sciences Director, Oncology
$211K - $285K *
Lead the charge in late-phase oncology clinical development, collaborating across teams to design and deliver impactful results. Provide expertise in clinical trial science and data analysis, ensuring...
Yesterday
Regulatory Affairs Consultant - CMC US/EU - Mature Biological products
$110K - $130K *
Transform global CMC regulatory strategies for biologics and vaccines, ensuring compliance and quality in submissions. Collaborate with cross-functional teams to influence outcomes and enhance patient...
1 week ago
Project Manager (Data Projects)
$120K - $125K *
Transform data analytics initiatives by leading multiple projects, engaging stakeholders, and driving solutions from inception to delivery. Collaborate with technical teams to ensure alignment with mi...
1 week ago
$90K - $140K *
Join our dynamic team as a Senior Medical Writer, where you'll lead the creation of critical regulatory documents for clinical trials, ensuring accuracy and compliance while managing client relationsh...
2 weeks ago
Experienced Clinical Project Manager - Inflammation (Sponsor Dedicated/ Remote- US only)
$110K - $130K *
Drive operational excellence in leading a complex Phase 2b inflammation study, overseeing clinical trial execution from start to finish. Collaborate with cross-functional teams in a fast-paced environ...
Reposted today
Experienced Clinical Project Manager - Inflammation (Sponsor Dedicated/ Remote- US only)
$110K - $130K *
Lead the charge in driving clinical trial execution for a complex Phase 2b inflammation study, ensuring operational excellence from start-up to closeout while managing cross-functional teams and exter...
Reposted 1 week 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.