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Clinical trial coordinator skills for your resume and career

15 clinical trial coordinator skills for your resume and career
1. Clinical Trials
- Assisted in depleting backlog of clinical trial complaints by effectively monitoring, researching, and analyzing complaint outcomes and summarizing reports.
- Supervised and coordinated clinical trials for Dr. Donald Black for his research in pathological gambling and borderline personality disorder.
2. Patients
- Verified patients' insurance eligibility and benefits for Medicare, Maryland state Medical Assistance and commercial insurances for all research participants.
- Facilitated the management in completing general formalities related to the patients, like insurance and medical reports generations.
3. Informed Consent
- Reviewed all study documentation, including informed consent.
- Administered the informed consent form, conducted patient visits, completed case report forms, and maintained regulatory documents.
4. 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.
- Reviewed protocol and prepared documentation for IRB initial approval and renewal.
- Updated and maintained IRB certification for Clinical Centers/Core Laboratories.
5. Meeting Minutes
- Organized and facilitated weekly Clinical Development Team meetings, recorded meeting minutes, and logged Action and Decision items for follow-up.
- Coordinate and prepare necessary materials for clinical trial meetings and transcribe and distribute meeting minutes.
6. 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.
- Experience in GCP-regulated environment protocols, FDA submissions and other Regulatory Agencies.
- Assisted in analysis of available financial data and impact on compliance with FDA Rule on Financial Disclosure by Clinical investigators.
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Patient care entails the diagnosis, recovery, and control of sickness as well as the maintenance of physical and emotional well-being through the use of healthcare providers' services. Patient care is described as services provided to patients by health practitioners or non-professionals under guidance.
- Review and process all clinically related patient care charges for payment by the grant as established by the contract.
- Monitored, analyzed and documented ECG data and made sound clinical judgment in relation to patient care.
8. CRA
The Community Reinvestment Act - CRA is a federal law that encourages federal reserves, financial institutions - certain insured custodians, savings banks, and other lenders to meet the borrowing needs of borrowers in all segments of the community.
- Managed the CRA team and served as main point of contact for study logistics and related questions including subject eligibility questions.
- Worked side-by-side with CRA (Clinical Research Associate) and assisted in some of their tasks.
9. Internal Audit
Internal audit is an evaluation process that ensures that a company's risk management, governing body, and other internal processes are running effectively. People who perform internal audits must be highly qualified, have experience, and knowledge to work accordingly with the international standards and the code of ethics.
- Prepared internal audits of patient files, clinical data and protocol adherence.
- Completed training to perform internal audits on all areas of the company.
10. Oncology
Oncology is defined as the facet of medicine that deals with cancer. Oncology also deals with the prevention and diagnosis of these diseases. A medical professional who has studied the discipline of oncology is referred to as an ‘oncologist'. An oncologist can further specialize in their discipline and become a medical oncologist, surgical oncologist, or radiation oncologist.
- Coordinated radiation oncology machine credentialing for over 30 NCI cooperative group studies.
- Selected by Division VP to attend ASCO 1997-2000 -Developed Reimbursement Protocol utilized by US Oncology Sales
11. Data Entry
Data entry means entering data into a company's system with the help of a keyboard. A person responsible for entering data may also be asked to verify the authenticity of the data being entered. A person doing data entry must pay great attention to tiny details.
- Complete data entry and queries of study activities onto case report forms and maintain database programs to track all study activities.
- Created and maintained Study databases and performed data entry.
12. Excellent Organizational
- Demonstrated excellent organizational skills and communication skills, with the ability to teach effectively within a small group setting.
- Demonstrated excellent organizational skills by tracking all project activities in project.
13. Data Collection
Data collection means to analyze and collect all the necessary information. It helps in carrying out research and in storing important and necessary information. The most important goal of data collection is to gather the information that is rich and accurate for statistical analysis.
- Assist with data collection responsibilities such as filing, evaluation, assistance w/analysis, and reporting for a variety of studies.
- Assisted in the coordination and data collection of the Insulin trials and prepared bio-statistical analysis.
14. Study Activities
- Maintained records of study activities, including case report forms, participant releases, participant files and casespecific documentation.
- Monitored study activities to ensure compliance with protocols relevant to federal and state regulatory and institutional policies.
15. PowerPoint
- Presented research concepts and data to scientific and general audience using MS Powerpoint.
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What skills help Clinical Trial Coordinators find jobs?
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What technical skills for a clinical trial coordinator 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 trial coordinators possess?
Research Professor Financial Engineering, Director Hanlon Laboratories, Director Financial Analytics program, Stevens Institute of Technology
List of clinical trial coordinator skills to add to your resume
The most important skills for a clinical trial coordinator resume and required skills for a clinical trial coordinator to have include:
- Clinical Trials
- Patients
- Informed Consent
- IRB
- Meeting Minutes
- FDA
- Patient Care
- CRA
- Internal Audit
- Oncology
- Data Entry
- Excellent Organizational
- Data Collection
- Study Activities
- PowerPoint
- Data Management
- Consent Process
- Study Protocols
- Clinical Sites
- HIPAA
- Consent Forms
- Study Procedures
- Clinical Research Studies
- IV
- TMF
- Institutional Review
- Clinical Operations
- Clinical Trial Management
- Federal Regulations
- CTMS
- CRO
- Electronic Data
- Clinical Data
- Vital Signs
- Hippa
- ECG
- Patient Enrollment
- Electrocardiogram
- Data Analysis
- EDC
- NIH
- Patient Recruitment
- IND
- Regulatory Compliance
- Study Sponsors
- Investigational Product
- EKG
- Medical History
- Study Subjects
Updated January 8, 2025