Clinical Project Manager Resume Samples - Page 3

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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.

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21

Clinical Project Manager Consultant

Phase I, II, III, IIIB, IV
Therapeutic areas: Oncology, Lymphoma, Solid Tumors, Breast Cancer, Gastroenterology-Irritable Bowel Syndrome (Zelnorm), Infectious Disease-Herpes, Pain Management.

  • Acted as a liaison between international and local operations groups, therapeutic areas, and departments for evaluation of new projects for phase I-IV clinical trials.
  • Facilitated timely study trial allocation and execution, attended clinical team meetings, and generated study reports using IMPACT.
  • Managed CROs study activities. Developed patient recruitment plans. Proactively planned for database locks. Reviewed data quality.
  • Overall responsibility for the uneventful operation of clinical trials. Provided input on protocol design, and project milestones. Planned, managed and coordinated study and project team activities to ensure trials met or exceed objectives. Supervised field based CRAs.
  • Managed project budget and authorized payments to investigators based on project milestones.
Candidate Info
11
years in
workforce
7
months
at this job
BS
Engineering Science
MS
Engineering Science
MBA
Management
22

Clinical Project Manager

  • Prepared clinical project timelines, set milestones and anticipated obstacles
  • Forecasted clinical product needs to for assigned protocols
  • Managed budgets, negotiated and tracked expenditures with external partners
  • Managed assigned Clinical Research Associates and Clinical Project Coordinators
  • Organized and conducted Investigator and Safety Monitoring Board meetings
  • Actively contributed to the preparation of clinical study reports
Candidate Info
8
years in
workforce
2
months
at this job
BA
Psychology
23

Clinical Project Manager

  • Provided leadership for clinical projects by directing the activities, training and development of clinical research associates and a CRO.
  • Created and executed a project schedule and revised as appropriate to meet the changing needs and requirements of each project.
  • Tracked project expenses and budget to ensure expectations remained on course.
  • Delivered engaging, informative and well-organized presentations and communicated
  • Prepared investigational plans consistent with Division goals and managed the final
  • Assisted investigators in the preparation of manuscripts for publication and presentations of clinical study results.
  • Approved key study documents including the consent form and case report form.
Candidate Info
16
years in
workforce
5
years
at this job
BS
Nursing
24

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
PhD
Health Science
25

Clinical Project Manager

  • Managed all clinical trial activities for rate control trials including protocol development, study reports, budgets, and audits, creation of request for proposals, review of vendor contracts, proposals and scope management
  • Participated in strategic planning meetings with co-developers of rate and rhythm control compounds internal cross-functional project team meetings
  • Reviewed and contributed to development of INDs, End of Phase II Briefing document, Investigator Brochures, and publications
  • Implemented data review and study report review guidelines for more efficient review
Candidate Info
19
years in
workforce
2
years
at this job
HS
High School Diploma
BS
Health Arts
26

Clinical Project Manager

Managed the investigative sites by discussing and resolving protocol, budget, enrollment and staffing issues

  • Ensured that the project status information was collected and distributed to upper management, the regulatory department and all study team members
  • Directed, interacted and trained the CRAs and project coordinators to ensure that the project was properly monitored and the data was accurate
  • Directed outside vendors including consultants and CROs with respect to the clinical trials
  • Prepared and reviewed protocols, CSRs, CRFs and other study information
  • Prepared and reviewed SOPs and ensured that procedures were appropriately and consistently applied to all study activities
  • Negotiated budgets/contracts with investigators
  • Developed monthly newsletters
  • Responsible for the timely completion of all studies
  • Assisted with the preparation of QA Audits
Candidate Info
21
years in
workforce
11
months
at this job
BS
Health Education
MS
Health Education
27

Clinical Project Manager

Implemented risk management measures to keep assigned projects in alignment with original goals in order to avoid delays to patient outcomes.

  • Planned, executed and assessed/revision of assigned programs/initiatives in support of MMRC's fundamental business strategy of bringing new cancer treatments to patients rapidly.
  • Tracked and reported MMRC trials to CMO/VP; driving site start up and enrollment plans on assigned trials.
  • Provided guidance to industry on the role of MMRC Operations including the importance of setting timelines and mutual expectations during early stage of protocol concept development.
  • Interacted with the CMO/VP/AD Ops, external vendors and site personnel i.e. investigators, MMPCs, their supervisors, to ensure MMRC's goals and objectives are met i.e. resolution of internal and external issues delaying rapid start up and enrollment.
Candidate Info
9
years in
workforce
6
months
at this job
BA
Political Science
Clinical Research
28

Clinical Project Manager

Provided disease management and physician profiling studies to health plans and outcomes studies for pharmaceutical companies.

  • Project Manager for new products with revenues ranging from $30,000 to $5 million
  • Training liaison for clinical methodology between developers, programmers, and clinicians
  • Managed client needs through initiating communications with clients, analysis of product intent and internal team building
  • Developed problem/solution database in Microsoft Access that resulted in faster deliverables, reduction of programming errors and system inefficiencies
  • Analyzed internal processes and developed solutions to provide efficiency improvements, cost savings, and improved associate knowledge of products
  • Provided training for clients on product software and health care analysis reports
  • Researched medical industry guidelines, trades and studies used to improve development and clinical validity of products
  • Developed company newsletter
  • Created and managed documentation for proprietary methodology
Candidate Info
7
years in
workforce
2
years
at this job
Physical Science
Project Management
29

Quality Manager / Clinical Project Manager

  • Provided project management and supervision for a professional research staff
  • Created and implemented a quality improvement program
  • Supervised the Transplant Case Management Department
  • Standardized workflows and instituted process improvement guidelines
  • Coordinated initiatives to combine evidence-based medicine with provider experience in development of Medical Policies and Utilization Guidelines
Candidate Info
24
years in
workforce
4
years
at this job
AS
Nursing
BS
Nursing
MS
Healthcare Administration
30

Clinical Project Manager

  • Co-developed and reviewed project budgets and timelines resulting in efficient, cost effective, on-time performance.
  • Managed clinical projects during entire life-cycle including recruitment, start-up, study participation, maintenance and closeouts using reporting tools to generate and follow project performance and trend analysis.
  • Developed and managed data collection for multiple clinical projects, NIH and other research and performed quality control review of collected data to ensure compliance with protocol requirements, domestic and global regulations to include CFR Part 11.
  • Designed and administered MS Access databases for data collection/management.
Candidate Info
4
years in
workforce
4
years
at this job
BS
Health Services Administration
MA
Master of Arts
MA
Information Systems

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