Clinical Project Manager Resume Samples - Page 5

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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.

41

Clinical Project Manager

Remotely manage all operations and conduct of global Phase III clinical trial(s) in Respiratory therapeutic area on high priority, large multi-center studies for sponsor company in 13 countries

  • Manage team members, regional monitors, vendors and CRO partners to ensure coordination of task delivery and proper resolution or escalation of issues and performance.
  • Identify and address all study, site and vendor related issues throughout all phases of trial management from study conception through reporting and submission.
  • Develop and maintain study timelines and clinical trial budget and studies financial reconciliations/payments
  • Ensure study inspection readiness and team member/partners adherence to protocol, sponsor SOPs and GCP/FDA regulations
  • Ensure timeliness, quality and integrity of study data
Candidate Info
37
years in
workforce
1
year
at this job
AS
Associate of Science
BS
Management
Applied Project Management
42

Contractor/senior Clinical Project Manager

  • Key responsibility of development, implementation and facilitation of clinical, and rater training programs for pharmaceutical clients.
  • Provided primary support for coordination of e-learning and on-site training for investigators, clinical team and site personnel.
  • Responsible for managing deployments, enhancements, defect resolution, eLearning integration and release management of Plateau LMS.
  • Developed and managed project timelines, deliverables, and site communication materials.
  • Worked in team environment and cross-functional activities related to patient recruitment and feasibility study projects.
  • Evaluated project outcomes and prepare evaluative reports.
Candidate Info
11
years in
workforce
9
months
at this job
43

Clinical Project Manager

  • Managed delivery of domestic and international cardiovascular safety monitoring services
  • Implemented project management plans and oversaw performance of internal project teams
  • Responsible for development and accuracy of project budgets and forecasts
  • Accountable for overall project team performance with respect to service delivery, quality and costs
Candidate Info
8
years in
workforce
2
years
at this job
BA
History (with Distinction)
MA
History (thesis
Clinical Trial & Therapeutic Experience
44

Clinical Project Manager

Management responsibilities for all aspects of Eclipsys/Allscripts full cycle delivery of multiple projects, i.e., activities related to the completion of this goal include responsibility for producing, monitoring, and reporting project status against project work plan as well as managing a project budget, resources, timelines, issues, and risks. Accountabilities and Responsibilities (90%+ national travel):

  • Manage project scope, implementation plan, and resources requirements for Eclipsys project team and client project team
  • Perform financial management, administration, and planning tasks that relate to client implementation projects.
  • Manage tasks associated with successfully implementing solutions at the client site (A/R)
  • Manage client relationships at the project and management level. Establish and maintain relationships with a diverse set of key clients, such as project office, I/T, clinical, and operational team leaders (A/R)
Candidate Info
26
years in
workforce
2
years
at this job
Management/labor Law
45

Clinical Project Manager

Perform neurological and genetic assessments on patients coming through the
Muscular Dystrophy and ALS clinics.

  • Manage multiple NIH-funded RO1 grants through the collection, compilation,
  • Develop and maintain regulatory compliance protocols, databases, forms,
  • Cultivate collaborations with investigators, local physicians, and clinics as well as procuring funds from non-profit foundations
  • Supervise multiple team members; participated in strategic planning and implementation of policies and community initiatives
Candidate Info
15
years in
workforce
7
years
at this job
BA
Psychology
BS
Nursing
MS
Nursing
46

Clinical Project Manager

Provide clinical and regulatory support for investigational diabetes device trials.

  • Oversee monitoring of study conduct, documentation, and protocol compliance
  • Oversee development of database, data entry and data verification
  • Assist with data analysis and writing of study reports
  • Provide primary technical support at study site
  • Ensure compliance with ICH GCP Guidelines, state and federal regulations
  • Assist with protocol, informed consent, and case report form development
Candidate Info
37
years in
workforce
6
years
at this job
BS
Education
MA
Nutrition
47

Clinical Project Manager

Responsible for the overall conduct of a trial, involved in the writing of protocols and amendments.

  • Responsible for managing the regulatory IRB/EC submissions.
  • Responsible for tracking patient enrollment.
  • Responsible for ensuring sites both domestic and international followed all ICH-GCP/European guidelines.
  • Responsible for assisting with the development of patient recruitment strategies and materials.
  • Liaison between Sponsor and CRO organizations.
Candidate Info
20
years in
workforce
3
years
at this job
BS
Biology
48

Clinical Project Manager

  • Current: Global Project Manager for a large Phase 3 study (23 countries and over 1000 subjects)
  • Manage cross functional teams through complete project life cycle from Feasibility to Close out (Clinical, Regulatory, DM, Safety, Medical, Third Party Vendors) within scope of work
  • Lead problem solving and resolution efforts to include management of risk, contingencies and issues.
  • Manage project finances and timelines.
  • Develop clinical reports and metrics including enrollment, and compliance metrics.
  • Lead and present project summary data at client meetings, medical monitor meetings.
Candidate Info
15
years in
workforce
7
years
at this job
MS
Electrical And Computer Engineering
PhD
Biomedical Engineering
Electronics Engineering

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