Clinical Project Manager Resume Samples - Page 4

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Clinical Project Managers usually work for pharmaceutical companies where they coordinate assigned clinical trials and complete tasks such as ensuring that projects are completed on time and within budget, creating timelines for each project, preparing documents, reviewing project tasks, handling budgets, and ensuring compliance with industry procedures and regulations. The ideal candidate should highlight in their resume thorough knowledge of clinical trial processes and medical terminology, and general business skills, such as communication, time management, and computer competencies. The most successful sample resumes showcase a Bachelor's or a Master's Degree in life sciences.

31

Clinical Project Manager

Served as lead project manager over full suites of clinical software solutions

  • Gathered client requirements for new clinical documentation products
  • Provided oversight in quality assurance testing
  • Managed activation planning and on site activation support
Candidate Info
4
years in
workforce
2
years
at this job
BS
Nursing
MS
Nursing
32

CRA, CRAII, Clinical Trial Manager, Clinical Project Manager

  • Established study milestones and ensured accurate tracking and reporting of study metrics
  • Performed ongoing vendor management (e.g., CROs, IVRS, imaging), including independent negotiation of scope of work, budgets, performance management, and issue resolution
  • Created and managed clinical education, staff and resource plans for more than 80 clinical protocols in Phase II, III and IV
  • Provided study-specific direction, generated performance reviews and mentored clinical trial coordinators and Specialist (CTS), provided support and mentored clinical trial regional managers
  • Ensured trial adherence to ICH/GCP/local regulations, participated in clinical operations initiatives, time lines and programs as assigned
  • Conducted more than 80 trials for (pacemakers, stents, catheters, adhesives, and CAPG) as well as pharmaceuticals (Oncology, Diabetes, Dermatology, Neurology, Transplant and General Practice)
  • Responsible for development and analysis of all study close out reports
  • Supervised a team of 74 investigators in an international trial for organ transplant registry study
Candidate Info
5
years in
workforce
5
years
at this job
BS
Biology
Doctor Of Chiropractic
33

Clinical Project Manager/clinical Trial Lead

  • Managed, monitored and coordinated the effort of clinical trial project teams
  • Conducted site assessments, including site recruitment and activation, interim monitoring and close- out visits for cardiac PET perfusion imaging studies
  • Performed co-monitoring visits in support of internal audits and project quality assurance activities
  • Supported the development of the project budget and scope of work
  • Conducted country level allocation including country and study level feasibility and assessments
Candidate Info
13
years in
workforce
9
months
at this job
C
Hospital Corpsman / Pharmacy Technician
BS
Workforce Education And Training
MS
Clinical Research Administration
34

Clinical Project Manager

Ensure that radiology and cardiology equipment are implemented in a timely and efficient cost minded manner according to scope for the clients.

  • This is accomplished by holding weekly or even daily team meetings per respective project stakeholders of each project whether it is regional or enterprise based.
  • Once all stakeholders are satisfied with project completion then the projects are closed and transitioned to support.
  • The projects are started and completed according to the stakeholder's needs and end of life requirements of equipment in the scope of the projects.
  • Meaningful use Medicare requirements are constantly being met in a timely manner.
Candidate Info
17
years in
workforce
3
years
at this job
BA
Management
MA
Business Management
Technology
35

Clinical Project Manager

  • Designed and implemented photographic protocols for major pharma clinical trials
  • Monitored and managed multiple studies and was the single point of contact for all study-related matters
  • Organized monitor reports and prepared PowerPoint presentations for investigator meetings
Candidate Info
8
years in
workforce
2
years
at this job
BA
International Relations
36

Clinical Project Manager Oncology

Conceived and wrote clinical study protocols with an appropriate methodology integrated from the clinical development plan and regulatory strategy

  • Quality Assurance Reviews of clinical development regulatory documents (i.e. briefing package, investigator brochure, protocols, etc.)
  • Coordinated all clinical and operational activities locally/globally within the planned time frame/budget and in the sought quality according to internal Standard Operating Procedures (SOP) and Good Clinical Practices (GCP)
  • Management of external vendors such as CROs and Central labs
  • Managed compliance of all submissions to the Clinical Trial Registry
Candidate Info
6
years in
workforce
4
years
at this job
BA
Clinical Research Science
MA
Clinical Administration
Clinical Project Management
37

Clinical Project Manager Global Evidence and Value Development, Global Medical Affairs

Lead the development, management and implementation of evidence generation strategies and deliverables to support the reimbursement, regulatory and business objectives during drug development

  • Developed strong understanding of global health care systems and built relationships with external Health Technology Assessment bodies/payer decision makers to garner insights into drug development
  • Managed external partners (CRO) relationships - reviewing proposals, creating SOW, monitoring ongoing activities, project timelines, liaison with internal stakeholders, metrics assessments, budget tracking
  • Managed global Health Technology Advisory Councils for payer insights into clinical development plan Worked in partnership with key internal and external stakeholders to ensure alignment of therapeutic area strategies to support internal decision making
  • Proactively educated internal matrix partners on evolving global payer/HTA needs to ensure buy in for proposed product development strategies
  • Key member of team for R&D portfolio evaluation (>100 indications) using novel multi-criteria decision analysis tool
  • Led the development and implementation of strategic action plan template
  • Ensured deliverables of high scientific quality, meeting internal and external quality standards
  • Spearheaded concept and developed executive project dashboard template for effective execution of project plans, resource allocation and processes refinement
Candidate Info
10
years in
workforce
10
months
at this job
C
Public Health
MA
Master of Arts
38

Clinical Project Manager

Optimize drug development by providing expert scientific input

  • Coordinate the planning and execution of multiple global Phase 3 Oncology trials
  • Direct resources, projects, ongoing trials and new trial star-ups
  • Manage study budgets and project timelines for global trials
  • Selected and managed multiple vendors at the study and corporate levels
  • Ensure studies are conducted within regulatory requirements, timeframes and budgets
  • Develop clinical protocols and study materials
  • Manage clinical operations team members
Candidate Info
30
years in
workforce
3
years
at this job
BS
Psychology
39

Clinical Project Manager

  • Handled a team of 4 people in clinical research department and assisted/analyzed their work to meet organization's objectives and goals
  • Directed an innovative Growth Hormone program for patients on dialysis suffering from complications related to diabetes
  • Worked with DaVita dialysis and large patient vendors to facilitate care and treatment
  • Managed budgets, staffing
  • Provided training and support to the team members
  • Responsible for recruiting for clinical research department
Candidate Info
14
years in
workforce
1
year
at this job
BS
Biology
MA
Population Dynamics / Reproductive Biology
Medical Humanities
40

Clinical Project Manager

  • Project Manager for leading IVRS Services Provider to the Pharmaceutical Industry; responsible for the direct management of a minimum of five (5) studies concurrently
  • Developed Project Specification and coordinate timelines for IVRS Platform design for pharmaceutical and biotech companies
  • Designed user friendly IVRS Programs (randomization, medication assignment and diary)
  • Coordinated client and internal validation (creation of validation plan, testing and reports for IVRS)
  • Investigator Meeting presentations
  • Oversaw and review data set releases for clients
  • Managed studies with complex randomization schedules (multiple stratum), med management, diary calls, diary data collection
  • Responsible for knowledge and adherence to 21 CFR PART 11
Candidate Info
5
years in
workforce
1
year
at this job
BA
Bachelor of Arts

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