Automatically apply for jobs with Zippia
Upload your resume to get started.
Senior clinical research coordinator skills for your resume and career
15 senior clinical research coordinator skills for your resume and career
1. Patients
- Managed three NIH funded studies including development and design of educational interventions for patients and caregivers.
- Compiled databases/CRF development for screening potential patients for clinical trials using REDCAP software from Vanderbilt University.
2. 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.
- Managed electronic database and responsible for protocol updating to IRB.
- Assisted in the in-house study protocols and protocol amendments, IRB submission, budget development, negotiation and protocol amendments.
3. Informed Consent
- Coordinated a study of bipolar children including preparing recruitment materials, screening potential study subjects, and obtaining informed consent.
- Demonstrate GCP by administering suitable informed consent process with an enhanced enrollment worksheet.
4. 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.
- Coordinated study visits including scheduling, administering medical screening, and data collection materials preparation for the study subjects and clinicians.
- Conduct data collection for faculty initiated retrospective and prospective research studies, and industry sponsored clinical trials.
5. Coordinators
- Provide mentoring support to other Bereavement Coordinators within Kindred at Home.
- Trained and mentored new clinical research coordinators.
6. Patient Care
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.
- Coordinate with pharmaceutical companies, vendors, and patient care facilities to ensure maximum protocol compliance.
- Coordinated studies within inpatient, outpatient care units in collaboration with health care personnel.
Choose from 10+ customizable senior clinical research coordinator resume templates
Build a professional senior clinical research coordinator 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 senior clinical research coordinator resume.7. Research Projects
- Coordinated and Managed Clinical Research Projects.
- Experience with developing local and nationwide physician networks for the purposes of subject recruitment and primary research projects.
8. Research Data
- Performed activities involved with the collection, compilation, documentation and analysis of clinical research data.
- Perform source document verification of protocol compliance and drug accountability prior to research data capture.
9. 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.
- Authored study specific documents according to FDA regulations.
- Coordinate and execute Phase II-IV clinical trials in accordance with FDA and Good Clinical Practice guidelines.
10. 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.
- Conducted training in conjunction with the Research Administration Training Series (RATS) in GCP and regulations.
- Coordinated multiple clinical research studies while adhering to Good Clinical Practice Guidelines (GCP).
11. Clinical Research Studies
- Coordinated and documented activities for clinical research studies.
- Coordinated multiple clinical research studies.
12. 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.
- Participated in complete process of clinical research trial management and coordination, IND safety reporting, QA and data entry.
- Complete Clinical Case Report Forms and use electric data entry for paper and for brain imaging scans.
13. 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.
- Collaborated with principal investigators and internal and external customers for effective execution of clinical trials in an oncology clinic setting.
- Coordinate 8 phase I-III, late stage melanoma clinical trials with oncology team, major pharmaceutical companies, and academic institutions.
14. CRC
- Support CRC's with any outstanding issues related to Trials.
- Train new site personnel Perform internal QA audits Additionally, perform all duties as described in below CRC description
15. Consent Forms
Consent forms refer to something that a person signs or attests to in order to agree for something that involves them to happen. They are used in various fields and applications. It is a legal document that can have repercussions if forged or denied later. In medical terms, it is the informed consent of the patient agreeing to the medical procedure they are about to undergo in a sound state of mind.
- Maintain consent forms and sponsor correspondences.
- Facilitated the review of investigative site consent forms and regulatory file reconciliation.
5 Senior Clinical Research Coordinator resume examples
Build a professional senior clinical research coordinator 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 senior clinical research coordinator resume.
What skills help Senior Clinical Research Coordinators find jobs?
Tell us what job you are looking for, we’ll show you what skills employers want.
What technical skills for a senior clinical research 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 senior clinical research coordinators possess?
Research Professor Financial Engineering, Director Hanlon Laboratories, Director Financial Analytics program, Stevens Institute of Technology
List of senior clinical research coordinator skills to add to your resume

The most important skills for a senior clinical research coordinator resume and required skills for a senior clinical research coordinator to have include:
- Patients
- IRB
- Informed Consent
- Data Collection
- Coordinators
- Patient Care
- Research Projects
- Research Data
- FDA
- GCP
- Clinical Research Studies
- Data Entry
- Oncology
- CRC
- Consent Forms
- Federal Regulations
- Data Analysis
- Vital Signs
- Study Subjects
- HIPAA
- Institutional Review
- NIH
- ICH
- Patient Education
- Study Procedures
- Consent Process
- Site Initiation
- Clinical Research Trials
- Clinical Trial Management
- CRO
- IP
- Laboratory Results
- ECG
- III
- IATA
- Regulatory Binders
- Medical Oncology
- EKG
- Subject Recruitment
- Neurology
- Regulatory Submissions
- IV
- CRF
- EDC
- Patient Recruitment
- Drug Accountability
- Medical History
- Phase II
Updated January 8, 2025