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Senior Clinical Research Manager
TFS HealthScience - Contract Research OrganizationSenior Clinical Research Manager providing clinical operations expertise to a biotechnology company. Supporting clinical development planning and study readiness in a growth phase with part-time commitment.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical operations and project management, with a strong focus on developing operational strategies and supporting clinical development plans. Proficient in stakeholder management and risk assessment to ensure efficient study execution.
Highest-signal resume keywords
Clinical OperationsClinical Trial ManagementICH-GCP KnowledgeStakeholder ManagementOperational Strategy Development
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
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Hard Skills
Clinical Project ManagementStudy PlanningResource ForecastingOperational Feasibility AssessmentBudget EstimationRisk IdentificationMitigation PlanningEarly-Phase Clinical Development
Soft Skills
Strong CommunicationOrganizational Skills
Industry Keywords
Life SciencesNursingPharmacyMedicineBiotechPharmaceuticalCROGlobal Regulatory Requirements
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Contribute to the development of operational strategies and clinical development plans for ongoing and future programs
- Support study planning activities, including timelines, resource forecasting, operational feasibility assessments, and budget estimates
- Provide guidance on CRO, vendor, and site selection strategies for future clinical studies
- Identify operational risks, key milestones, and mitigation plans to support efficient study execution
- Collaborate with internal and external stakeholders to support clinical development planning and future study readiness
Requirements
What you’ll need- Degree in Life Sciences, Nursing, Pharmacy, Medicine, or a related healthcare field
- Significant experience in clinical operations, clinical trial management, or clinical project management within biotech, pharmaceutical, or CRO environments
- Strong knowledge of ICH-GCP, clinical trial conduct, and global regulatory requirements
- Experience supporting early-phase clinical development programs and study planning activities
- Strong communication, stakeholder management, and organizational skills
Benefits
Comp & perks- Opportunities for personal and professional growth in a rewarding environment
- Join a team that values collaboration, quality, and making a difference in the lives of patients