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Senior Manager, Patient Recruitment & Retention
AmgenManage patient recruitment and retention strategies for decentralized clinical trials at Amgen. Collaborating with clinical program teams and advocating for innovative solutions.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in developing and executing patient recruitment and retention strategies, as well as decentralized clinical trial methodologies. Proficient in managing clinical trial operations, including feasibility assessments and performance metrics analysis.
Highest-signal resume keywords
Patient Recruitment And RetentionDecentralized Clinical TrialsClinical DevelopmentData Analytics ToolsICH-GCP Compliance
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Trial OperationsStudy FeasibilityEnrollment PlanningRecruitment Risk MitigationProcess ImprovementsPerformance Metrics Analysis
Soft Skills
CollaborationAdvocacyRisk Management
Tools & Technologies
Data Analytics Tools
Industry Keywords
PharmaceuticalBiotechnologyCROHealthcareClinical Research Regulations
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Own the development and execution of the patient recruitment & retention (PRR) and decentralized clinical trial (DCT) strategies
- Lead the identification, selection, and onboarding of the most suitable partners or solutions
- Collaborate with cross-functional stakeholders for seamless integration of PRR and DCT elements into clinical trials
- Advocate for adoption of innovative PRR approaches and DCTs
- Identify and evaluate suitable technologies and vendors for PRR and DCT implementation
- Develop and manage feasibility assessments for trial protocols and sites
- Author PRR and DCT elements into protocols with regulatory teams
- Manage and monitor PRR & DCT execution utilizing data analytics tools
- Identify and manage potential risks associated with PRR & DCTs
- Stay informed of the latest trends and regulations in PRR & DCT solutions
- Analyze and report on PRR & DCT performance metrics.
Requirements
What you’ll need- Doctorate degree and 2 years of relevant experience OR Master’s degree and 4 years of relevant experience OR Bachelor’s degree and 6 years of relevant experience OR Associate’s degree and 10 years of relevant experience OR High school diploma / GED and 12 years of relevant experience
- Bachelor's degree in Life Sciences, Public Health, Clinical Research, Healthcare, or a related field preferred
- 5+ years of experience in clinical development, clinical operations, patient recruitment and retention, or related functions within the pharmaceutical, biotechnology, CRO, or healthcare industry
- Understanding of clinical trial operations, including study feasibility, enrollment planning, patient burden reduction, and recruitment risk mitigation
- Experience using operational data and performance metrics to monitor recruitment progress and inform decision-making
- Knowledge of ICH-GCP, applicable clinical research regulations, and patient privacy requirements
- Experience driving process improvements, developing best practices, and scaling capabilities across multiple studies.
Benefits
Comp & perks- A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions
- Group medical, dental and vision coverage
- Life and disability insurance
- Flexible spending accounts
- A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
- Stock-based long-term incentives
- Award-winning time-off plans
- Flexible work models where possible.