Automatically apply for jobs with Zippia
Upload your resume to get started.
Clinical project manager skills for your resume and career

15 clinical project manager skills for your resume and career
1. Manage Cross
- Develop and maintain project schedule, identify and track milestones and identify and manage cross-functional dependencies.
- Manage cross-functional teams to achieve project milestones and other project approved objectives.
2. Patients
- Collaborated with sponsors, reader groups, stakeholders, vendors, clients, project staff and patients.
- Championed an incentive program to encourage use of services and bring more patients in for consulting.
3. Clinical Research
- Manage Clinical research associate resignations and releases by working with clinical resourcing to ensure primary sites are covered and reassigned.
- Directed work with Clinical Research Statistician for statistical development and power for positive/successful results of clinical research project.
4. Project Management
- Presented on a monthly basis to senior management regarding departmental development and the status of ongoing project management initiatives.
- Project Management, eliciting product requirement, producing design requirement documentation and managing development of product through implementation
5. Clinical Trials
- Headed Clinical Trial Material Coordination and Communication team for effective planning of upcoming and existing clinical trials within Eli Lilly.
- Displayed unsurpassed management expertise in the entire clinical trial process, including tracking of enrollment projections and sites activation.
6. Oversight
Having oversight of someone means to monitor a process or a situation. If someone has oversight of something, they are responsible for the completion of the project. Oversight is usually given to experts as they monitor their juniors or newbies as they go through a project.
- Ensured appropriate clinical safety assessment and risk management of compounds, conducted real-time medical oversight of ongoing trials.
- Provided leadership and strategic oversight of top-priority clinical programs.
Choose from 10+ customizable clinical project manager resume templates
Build a professional clinical project manager resume in minutes. Our AI resume writing assistant will guide you through every step of the process, and you can choose from 10+ resume templates to create your clinical project manager resume.7. CRO
A CRO (Cathode Ray Oscilloscope) refers to an electrical device usually used in a laboratory to exhibit, measure, and analyze different waveforms of electrical circuits.
CRO may also refer to Conversion Rate Optimization -- the practice of improving a process or product to maximize the number of conversions or sales.
- Supervised rotating team of CRA's contracted with the CRO, educating on therapeutic area, and ensuring ICH GCP compliance.
- Served as a liaison between Contract Research Organizations (CRO), clinical sites, investigators/key opinion leaders and marketing teams.
8. FDA
The Food and Drug Administration (FDA) is a division of the US Department of Health and Human Services that regulates the production and sale of food, pharmaceutical products, medical equipment, and other consumer goods, as well as veterinary medicine. The FDA is now in charge of overseeing the manufacture of products like vaccines, allergy treatments, and beauty products.
- Monitored clinical investigations by performing on-site visits to assure medical accuracy and compliance with protocol, ICH/GCP guidelines and FDA regulations.
- Managed multiple pharmaceutical studies ensuring compliance with FDA guidelines.
9. Clinical Operations
Clinical operations caters to the administration of the drug development process by ensuring there is proper planning, appropriate conduct through the process, safety of patients and use of quality data. It also encompasses facilitating effective communication between the different study sites and sponsors of the drug process.
- Represent Clinical Operations on several committees and task forces during the implementation of new processes and reorganizations of functional departments.
- Help facilitates information flow between all members of the clinical operations/clinical trial project team both domestic and globally.
10. Data Management
The administrative process that involves collecting and keeping the data safely and cost-effectively is called data management. Data management is a growing field as companies rely on it to store their intangible assets securely to create value. Efficient data management helps a company use the data to make better business decisions.
- Coordinated all data management aspects of assigned protocols and provided any data to sponsors as needed within a timely manner.
- Supervised research assistants and data entry personnel and monitored data management work done by outside vendors.
11. Clinical Project
- Defined project scope, developed detailed project plans and conducted project meetings for all assigned clinical projects using Waterfall project methodology.
- Collaborated with the client's multidisciplinary clinical team throughout the analysis and development of clinical projects.
12. Process Improvement
- Facilitated process improvement efforts both within the department and in cooperation with other departments.
- Participate in process improvement delegations to reduce errors, increase efficiency and establish goals.
13. Ich
- Conducted studies in keeping with GCP/ICH and HIPAA standards.
- Ensured site compliance with study protocols, SOPs, applicable regulations, ICH and GCP.
14. GCP
Google Cloud Platform (GCP) is a collection of cloud computing services that allow users to develop, deploy, and operate original applications on the web. GCP carries a cloud computing infrastructure that facilitates it in keeping track of the resources (e.g., storage, processing speed, and power, network connectivity, database queries, etc.) of an application or a website, whenever it is run on the cloud platform.
- Reviewed investigative sites' regulatory documentation and ensured compliance with GCP.
- Initiated actions to ensure all assigned investigative sites were in compliance with protocol and GCP.
15. IRB
An institutional review board (IRB), is a form of committee that applies research ethics by vetting research procedures to ensure they are ethical. In order to decide whether or not research can be undertaken, they often perform a kind of risk-benefit analysis. The IRB's function is to ensure that adequate safeguards are in place to protect the interests and health of humans who are participants of a research sample.
- Handled direct communication with IRB for complete submission and maintenance of essential regulatory documents.
- Coordinated site initiation meetings, prepared IRB documents, developed documents and routing slips, and reviewed protocols and consent forms.
5 Clinical Project Manager resume examples
Build a professional clinical project manager resume in minutes. Browse through our resume examples to identify the best way to word your resume. Then choose from 5+ resume templates to create your clinical project manager resume.
What skills help Clinical Project Managers find jobs?
Tell us what job you are looking for, we’ll show you what skills employers want.
What technical skills for a clinical project manager stand out to employers?
Assistant Professor of Spanish, Foreign Languages Division Coordinator, Faculty Affiliate, Center for Critical Race & Ethnic Studies, Florida Gulf Coast University
What soft skills should all clinical project managers possess?
Research Professor Financial Engineering, Director Hanlon Laboratories, Director Financial Analytics program, Stevens Institute of Technology
List of clinical project manager skills to add to your resume

The most important skills for a clinical project manager resume and required skills for a clinical project manager to have include:
- Manage Cross
- Patients
- Clinical Research
- Project Management
- Clinical Trials
- Oversight
- CRO
- FDA
- Clinical Operations
- Data Management
- Clinical Project
- Process Improvement
- Ich
- GCP
- IRB
- Patient Care
- Clinical Practice
- Site Management
- Informed Consent
- IDE
- Oncology
- Manage Change
- Excellent Interpersonal
- Study Timelines
- Consent Forms
- Clinical Trial Management
- Data Collection
- Clinical Data
- CRAs
- Study Protocols
- Regulatory Submissions
- IV
- Clinical Sites
- Data Analysis
- Principal Liaison
- Project Scope
- Study Start-Up
- Standard Operating Procedure
- Team Training
- Direct Reports
- CRF
- QA
- Pharmaceutical Industry
- Site Selection
- Investigative Sites
Updated January 8, 2025