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Senior research coordinator skills for your resume and career
15 senior research coordinator skills for your resume and career
1. Patients
- Created and maintained Access database to track and monitor clinical research studies, patients enrolled and outcomes.
- Created and composed Excel Spreadsheet for PI weekly GVHD meeting to review the pathology of patients.
2. 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 data collection, scheduled appointments, obtained consent, and completed research study procedures with precision and followed research protocol.
- Performed data entry and data collection for renal research protocols in compliance with all regulatory, institutional and departmental requirements.
3. 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.
- Assisted the PI in obtaining and updating all site-specific study requirements, including IRB submissions, updates and revisions.
- Monitored Adverse Events and Serious Adverse Events and report them to the Sponsor and IRB per the CP guidelines.
4. Research Projects
- Coordinated 5-7 research projects to ensure compliance with all regulatory, institutional, and departmental requirements.
- Completed primary and secondary market research projects as assigned.
5. Data Analysis
- Assist with the data analysis by using statistical packages.
- Developed sampling procedures and conducted data analysis to support research involving children with Cranio-facial Anomalies and adult victims of facial trauma.
6. Informed Consent
- Prepare informed consent forms for study participants.
- Worked independently providing study coordination, including screening of potential patients for protocol eligibility and participating in the informed consent process.
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- Coordinated multiple clinical trials and academic studies.
- Developed and conducted training programs to train physicians, nurses and research assistants on subject recruitment for various clinical trials.
8. 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.
- Designed and implemented clinical quality and research data management systems using Research Electronic Data Capture.
- Provide data entry and data management for assigned protocols.
9. 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.
- Coordinated data entry and ensured data quality.
- Coordinated data cleaning and data entry for nutrition and fitness projects.
10. Research Data
- Developed and maintained research database.
- Assist with interview process for the position of Research Data Coordinator at the MD Anderson Proton Therapy Center - Houston.
11. 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.
- Entered patient data per visit requirements and maintained proper consent forms necessary for patient participation in studies.
- Provided hands-on guidance to research study teams on protocol and consent form development to ensure compliance with institutional and federal requirements.
12. Study Protocols
- Assisted researchers in developing study protocols and matched available tissues with individual tissue requests.
- Maintained good working knowledge of all assigned study protocols and reporting requirements.
13. Principal Investigators
A principal investigator is an individual who's responsible for preparing, conducting, and overseeing a sponsored project, research grant, training, contract,or any project in line with the regulations and instituted laws guiding the conduct of a sponsored research. It majorly applies to research projects, and the PI or principal investigator ensures everything is fully supervised to align with the laws of a sponsored research project.
- Participated in site development and start up meetings with principal investigators and sponsoring agencies.
- Established strong service relationships with Principal Investigators, Clinical Research Staff, and Sponsors for smooth protocol execution and communication.
14. Research Assistants
- Managed research assistants by instituting and teaching project management standards and high-quality, client-ready deliverable production.
- Supervised undergraduate research assistants and effectively coordinated assigned tasks to facilitate progress.
15. Clinical Data
- Developed and maintained a complete, accurate clinical database including the processing of CRF's data queries and data audits.
- Developed clinical database and the maintenance (including, but not limited to archiving) all EMG data.
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What skills stand out on senior research coordinator resumes?
Professor, Department Chair, The University of Iowa
What senior research coordinator skills would you recommend for someone trying to advance their career?
Professor, Ohio State University
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Associate Professor of Environmental History, Ohio State University
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Assistant Professor of Spanish, Foreign Languages Division Coordinator, Faculty Affiliate, Center for Critical Race & Ethnic Studies, Florida Gulf Coast University
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Assistant Director, Graduate Education & Career Connections, Morehouse School of Medicine
List of senior research coordinator skills to add to your resume
The most important skills for a senior research coordinator resume and required skills for a senior research coordinator to have include:
- Patients
- Data Collection
- IRB
- Research Projects
- Data Analysis
- Informed Consent
- Clinical Trials
- Data Management
- Data Entry
- Research Data
- Consent Forms
- Study Protocols
- Principal Investigators
- Research Assistants
- Clinical Data
- Clinical Practice
- PowerPoint
- Institutional Review
- FDA
- NIH
- Literature Reviews
- SAS
- Vital Signs
- Federal Regulations
- Statistical Analysis
- GCP
- HIV
- Visualization
- Clinical Research Studies
- PIS
- Study Subjects
- Participant Recruitment
- Regulatory Agencies
- Hippa
- Regulatory Compliance
- Extraction
- Study Sponsors
- Electronic Data
- Standard Operating Procedure
- CRF
- Subject Recruitment
- Clinical Trial Management
Updated January 8, 2025