Senior Clinical Trials Manager
15 Sep 2025
Watertwon
Verified by Turrior
Content + Source + Freshness • 12 Dec 2025 • 95% confidence
80 / 100
Offer value
High value due to demand for clinical management roles and significant responsibility in trial execution.
- Leads high-impact clinical trials
- Competitive compensation and benefits
- Requires significant clinical research experience
Pros
- Leadership position with direct influence on clinical trials.
- High demand in the biotech industry for experienced managers.
- Opportunity for career growth with project management experience.
Cons
- Requires substantial experience in clinical trial management.
- Often involves long hours with tight deadlines.
- Frequent collaboration with multiple stakeholders can be challenging.
Who it's for
Mid to Senior-level • On-site
Good fit
- Experienced clinical trial managers
- Professionals in the biotech research sector
- Candidates eager for project leadership roles
Not recommended for
- Newcomers to clinical trial management
- Individuals seeking remote work arrangements
- Those uncomfortable with collaborative project environments
Motivation fit
Interest in advancing clinical research.Desire to lead and manage multi-faceted projects.Commitment to ensuring trial data integrity.
Key skills
Project management and team leadership.Clinical research regulations and protocols.Analytical skills for data interpretation.
Score: 80/100 AI verified analysis
About the job
How you’ll make an impact:
- Contribute to the planning, implementation and execution of a global clinical trial
- Responsible for management of vendors to support clinical trial execution
- Plan, execute, and lead study-specific meetings (e.g., internal core team meetings, investigator meetings, etc), as needed
- Provide input for the design of the Informed Consent Form(s), eCRFs, monitoring conventions, edit checks, etc.
- Provide study-specific training and leadership to clinical research staff, CRO, CRAs, sites and other contract personnel.
- Manage study timelines and metrics to ensure completion of study deliverables
- Support site selection, qualification, initiation, and monitoring activities.
- Review monitoring reports to ensure quality and resolution of site-related issues.
- Ensure timely enrollment and data collection at clinical trial sites.
- Collaborate with the data management team to ensure data integrity and timely database lock.
- Review and analyze clinical trial data to identify trends and potential issues.
- Ensure tracking and review of protocol deviations and assess impact on study data
- Develop relationships with investigators and site staff
- Work closely with CRO and Medical Monitor to ensure safety and efficacy data appropriately summarized to facilitate review.
- Work closely with translational medicine team to ensure appropriate incorporation of bioanalytical sampling plan into clinical protocols and relevant data output of the trial is provided to functional groups for review.
- Maintain accurate and complete trial documentation.
- Proactively identify and resolve clinical project issues.
Skills and experience you’ll bring:
- Bachelor of Science in Life Sciences and 5+ years as a Senior Clinical Trial Manager in the biotech/pharmaceutical industry.
- Experience working on large, global, complex phase 2b/3 or late stage trials. Respiratory or Immunology experience highly preferred.
- Broad knowledge of regulatory and ICH GCP guidelines, HIPAA, Protection of Human Research Subjects.
- Strong project management skills with the ability to manage multiple trials simultaneously.
- Excellent problem-solving, leadership, and communication skills.
- Ability to work in a fast-paced, dynamic environment with cross-functional teams.
