Write a targeted resume if you you want to apply for a new job as a clinical research manager. Targeted resumes are successful for a reason. They “target” the employer’s needs specifically and make the candidate come across as someone they were looking for all their lives. The beauty of a targeted resume lies in the fact that they are exactly what the employer needs, which makes it easier for candidates to reach the interview stage.
Standardized resumes do not do this. While some standardized ones are actually quite informative, mostly, they fail to impress. Verdict? Always write a targeted resume.
Look at the sample below to get a better idea.
Clinical Research Manager Resume Sample
Christopher Webb
88 E Park Avenue | Ranson, WV 66534 | (000) 999-8754 | christopherwebb @ email . com
Clinical Research Manager
Performance Profile/Performance Summary
• Detail-oriented, highly-motivated Clinical Research Professional with 8+ years’ successful track record of developing project plans and schedules to document project goals and objectives. Demonstrated ability to provide administrative and research support and direction to clinical operations, and leading activities related to the development and execution of cross-functional and third party deliverables.
• Competent in maintaining oversight of operational aspects of clinical projects and ensuring compliance
• Proven ability to organize tracking, management and reporting of clinical study budgets
Clinical Research Skills
| • Human research subject protection | • Data collection |
| • Clinical site identification | • Clinical monitoring |
| • Vendor management | • Project timelines |
| • SOPs development | • Post-clinical activities support |
| • Informational analysis | • Data review |
| • Trial operations management | • Budget development |
Key Accomplishments
• Created and implemented a clinical investigation plan which increased efficiency by 50%
• Trained 15 research assistants in handling site initiation, closeout and interim monitoring work
• Introduced 8 different clinical trial committees, including clinical events committee, data safety monitoring board and steering committee
• Obtained 3 informed consents for human research subjects which were in limbo for 5 years
PROFESSIONAL EXPERIENCE
Progyny, Ranson, WV 2012 – Present
Clinical Research Manager
• Prepare protocols and case report forms to increase patient randomization
• Coordinate the smooth monitoring of all trials through identification and management of qualified staff
• Participate in global clinical research work and ensure that coworkers are updated of progress
• Handle financial management of clinical trial programs including budget management and resource allocation
• Implement training programs for staff members and handle budget control and reporting activities
Progyny, Ranson, WV 2008 – 2012
Clinical Research Assistant Manager
• Monitored the progress of project deliverables
• Highlighted potential hazards so that they can be addressed in a time efficient manner
• Performed reviews of site visit reports and ensured proper resolution of outstanding issues
• Ascertained that relevant study information was communicated across the panel in an eloquent manner
• Oversaw the development and content of study manuals and plans
Lifespan, Ranson, WV 2005 – 2008
Clinical Research Assistant
• Coordinated communications around team projects to ensure that processes and logistics were managed properly
• Generated invoices and track payments for both external and internal projects
• Created budget documents for clinical research projects and perform necessary audits of all research efforts
• Organized research meetings and provided administrative support to all aspects of clinical research trials
EDUCATION
Master of Science in Biological Sciences
West Virginia State University, Ranson, WV – 2004