A Research Study Coordinator is a specialized researcher who supports the coordination and management of clinical research or research studies. Job duties commonly listed on the Research Study Coordinator Resume include the following – managing the daily activities of clinical research; coordinating clinical or research studies to ensure the research complies with federal guidelines and institutional policies; ensuring proper training of research personnel and complying with federal guidelines; recording and documenting training activities of personnel; and documenting breach in compliance with federal and agency regulations.
Skills commonly highlighted on resumes include the following – knowledge of budgeting and financial principles; critical thinking skills; attention to details; ethical work practices; and excellent research skills. while education requirements depend on the area of research, most of these coordinators often possess a degree in relevant fields.
Objective : A self-directed, highly motivated individual, and innovative thinker for developing creative solutions to complex problems. Seeking a position with the opportunity for new challenges, professional development, and advancement. Passionate and driven when it comes to event planning, community engagement, and fund development.
Skills : Microsoft Office, EPIC EMR, OPEN EMR.
Description :
Identified appropriate subjects for research participation in lung transplant study, obtain informed consent and enroll patients in the study, process and ship lab samples, input data in online case record forms, communicate with a sponsor, facilitate monitored visits.
Prepared Human Subjects renewals and modifications.
Communicated with the Human Subjects Review Board.
Assisted with archiving of 42 cardiothoracic studies including file organization, contacting sponsors, creating a database of closed studies, communicating with IRB and administration.
Identified appropriate subjects for research participation in advanced heart and lung disease study, enroll eligible patients in the study, prepare Human Subjects applications, write consent forms, obtain informed consent, and submit protocols and modifications to Human Subjects Review Board.
Conducted and detailed and sensitive qualitative interviews by phone concerning patient and spouse's views of their illness and the end of their lives; apply advanced knowledge of cardiovascular nursing to assess patient reaction to their illness and its treatment within the research parameters to the principal investigator.
Coordinated and evaluated the collection of research data, arrange for interview transcription, entry into qualitative analysis software, and analyze data with guidance of principal investigator.
Experience
2-5 Years
Level
Executive
Education
Master Of Arts In Education
Research Study Coordinator Resume
Headline : A Certified Research Study Coordinator Professional that is highly focused on the improvement of the health delivery system. Highly analytical, with excellent communication and interpersonal skills, I am also passionate about contributing to better health outcomes and excellent quality of life.
Skills : Phlebotomy, MS Office, Training SKills.
Description :
Coordinated and performed screening, enrollment, and study visits.
Administered cognitive and clinical assessments on participants for Alzheimer's research studies.
Reported adverse events (AEs) and severe adverse events (SAEs) Maintained regulatory documents and files.
Prepared grants and grants report writing for sponsors.
Trained and supervised students and volunteers.
Maintained certification in the CITI continuing education course in the protection of human subjects.
Conducted clinical research studies under the supervision of the Principal Investigator.
Attended and participates in Investigator and staff meetings. Advises the team regarding specific study assignments and timelines.
Experience
5-7 Years
Level
Executive
Education
GED
Research Study Coordinator Resume
Objective : Dedicated and highly efficient Research Study Coordinator, currently responsible for the Cardiology research department with the nurse and non-nurse coordinators, research assistants, and regulatory staff members. I effectively manage all contracts, budgets and assignments for this large department, while also maintaining successful enrollment and patient management of my own assigned trials.
Skills : MS Office, Computer, SPSS, Meditech, Avatar.
Description :
Involved in multiple clinical research studies includes; CAROLINA: Cardiovascular Outcome Study of Linagliptin versus Glimepiride in Patients with Type 2 Diabetes.
Pre-screened of the patient via telephone or online.
Screened patients for a clinical trial, take a complete medical history, vitals, EKG, blood is drawn, and sample processing, a shipment of the sample, and any test procedures related to a clinical trial.
Maintained protocol requirements for patient visits, patient scheduling, test procedures, and drug accountability requirements.
Scheduled the patients for follow up visits and gave them follow up calls for any new changes noticed during that period.
Completed all study documentation forms like consent form, medical release form adverse report forms, and other specific research documents.
Processed payments for research participants per study protocol.
Experience
2-5 Years
Level
Executive
Education
MS
Research Study Coordinator Resume
Summary : A self-motivated and organized Research Study Coordinator with over 10 years of experience. My experience has led me to have extensive knowledge of good clinical practices, and industry regulations.
Skills : Clinical Research, Acute Health Care, Public Health.
Description :
Participated in the planning & conduct of research study including participant recruitment and retention.
Obtained informed consent.
Administered tests &/or questionnaires following protocols.
Completed basic clinical procedures such as drawing blood & obtaining blood pressure.
Experience
10+ Years
Level
Senior
Education
G.E.D
Research Study Coordinator Resume
Objective : Analytical and solution-focused Research Study Coordinator professional with over eight years of experience in the healthcare industry that possesses a strong combination of organizational abilities in clinical studies, including collection of clinical data, ICH guidelines, Title 21, SOP, submissions of data to sponsors and/or IRB, thorough and sensitive interaction with patients, scheduling of procedures, prepared specimens for analysis, dispensed study pharmaceuticals and facilitate principal investigator with a review of data.
Skills : Training Skills, Designing Skills, Analyzing Skills.
Description :
Supervised and managed the research programs.
Assisted with the writing of reports for Internal Review Boards, project sponsors, and others.
Participated in manuscript preparation and grant proposal writing.
Assisted with grant submission and management.
Designed and maintained databases on scientific literature, projects, and programs.
Prepared complex charts, data tables, and presentations.
Assisted with data management and analyzing data using ArcGIS.
Experience
2-5 Years
Level
Executive
Education
MS
Research Study Coordinator Resume
Headline : Proven Research Study Coordinator professional and dedicated team player with strong organizational, interpersonal, and communication skills. Collaborative with an ability to get along with others while working independently. Emotionally intelligent, faithful, and zealous to detail with a strong aptitude for Science. Enthusiastic about meeting deliverable timelines through diligence and merit.
Prepared reports for investigators and sponsors on recruitment status and other pertinent study data.
Wrote portions of grant applications & co-author scientific papers.
Completed documents associated with current local, state, & federal regulatory guidelines, requirements, laws & research protocols.
Worked with industry representatives to negotiate tentative grant funding.
Coordinated reimbursements for expert panel travel, consultant pay, additional gift card orders, etc. & ensure costs remain within allotted grant budget.
Experience
5-7 Years
Level
Executive
Education
G.E.D
Research Study Coordinator Resume
Objective : As a Research Study Coordinator, responsible for Reporting and tracking adverse events (AE). Reports serious AEs to IRB and sponsor, and also Documenting all protocol deviations, reconciles test article accountability at study close out and prepares a summary report for sponsor.
Prepared study participants for clinical research visits.
Provided work direction &/or train other research staff to interview/test participants.
Acted as a mentor in regard to the education of junior coordinators.
Assessed protocol for clarity and subject safety, reviews inclusion/exclusion criteria.
Clarified concerns and questions with the Principal Investigator and sponsor.
Explained and obtained informed consent, medical history, and demographics.
Documented in the source file and maintains historical data, status reports, progress notes, and subject logs to help ensure subject safety.
Experience
2-5 Years
Level
Executive
Education
G.E.D
Research Study Coordinator Resume
Objective : As a Research Study Coordinator, responsible for Participating in the planning & conduct of research studies, and also Reviewing project & protocol & recommends strategies to expedite study, Recruiting & retaining participants.
Skills : Instructing Skills, Coordinating Skills, Communication Skills.
Description :
Communicated with sponsors, faculty, and staff as well as other internal and external constituencies.
Maintained research project budgets.
Conducted literature review, assist in the preparation of data for use in manuscripts for a professional publication, assist in writing grants, and developing budgets.
Instructed hospital and clinic staff in the implementation of the research protocol.
Prioritized multiple tasks in order to achieve project timelines.
Took initiative to achieve task resolution by working independently or within a matrix environment.
Studied startup with a budget review, protocol review, and sponsor regulatory required reports.
Experience
2-5 Years
Level
Executive
Education
Teaching Scholarship Webinars
Research Study Coordinator Resume
Objective : As a Research Study Coordinator, responsible for Assisting Investigators by reviewing, editing, and preparing documents including budgets for grant/ contract proposals, application forms, contracts and agreements, no-cost extensions, etc. Experience in Coordinating proposal and subcontract preparation, grants and contract transfers, etc.
Skills : MS Office, Planning, Monitoring.
Description :
Analyzed and developed a study design.
Independently managed all phases of studies complying with regulatory laws and institutional guidelines.
Served as an expert resource and mentors another internal and external study/protocol personnel.
Knowledgable of Mayo IRB policies and federal regulations related to research involving human subjects.
Contributed to discussions on research study design overall project management and study results.
Participated in designing, organizing, and monitoring protocol including budget elements.
Planned for and participates in the education of staff areas required to carry out the protocol.
Experience
2-5 Years
Level
Executive
Education
BA
Research Study Coordinator Resume
Objective : Seeking a Research Study Coordinator position, responsible for Engaging in outreach and field relations serving a number of goals, including recruitment, participation, sponsorship, relationship building, etc. to support continued program/project development & improvement.
Skills : Research coordinator, COmmunication, Detail-Oriented.
Description :
Led study management activities, including budget/contract negotiations, maintenance of Confidential Trial Agreements (CTA), and direct correspondence with the sponsor.
Oversaw document maintenance services, including protocol-related invoices, receipts, and payments for study reimbursements.
Facilitated and tracked patient compensation for study-related visits.
Ensured completion of study start-up documentation, such as Institutional Review Board (IRB) submissions and study-related communications, IVRS startup, EDC implementation, and entry guidelines, and source documentation format creation.
Acted as point-of-contact for sponsors and relay pertinent information to Principle Investigator.
Expedited query resolution and maintain tracking documentation.
Ensured adherence to Good Clinical Practice (GCP) Principles.
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