Research Coordinator Resume Samples

Description :

1. Researched, collected, and analyzed data and statistics related to the prevention of communicable diseases and the promotion of positive health outcomes.
2. Supervision and training of research assistants in human subjects research protocols, qualitative focus group facilitation skills, and quantitative survey collection and analysis techniques.
3. Research, development, and implementation of specific research policies and protocols for public health studies on health promotion and disease prevention.
4. Served as the University of Nevada, Reno School of Community Health Sciences' community liaison on several advisory boards and coalitions, including the Maternal Child Health Coalition and the Northern Nevada HIV/AIDS Prevention Planning Council.
5. Curriculum development, instruction assistance, and evaluation studies of six undergraduate courses in public health, including courses related to maternal-child health, chronic disease prevention, and communicable disease prevention.
6. Conducted outreach, presentations, and community engagement initiatives to nontraditional partners in order to improve research participation and community advisory board participation for projects related to health promotion and disease prevention.
7. Research, submission, and publication of peer-reviewed conference abstracts and research articles related to the prevention of communicable diseases among vulnerable populations.
8. Skills Used Research, professional presentation skills, supervisory skills, time management, communication.

Experience

2-5 Years

Level

Executive

Education

Public Health

Description :

1. Assists in planning and coordinating the initiation of research study protocol, and the establishment of operating policies and procedures.
2. Assists in planning, implementing, and maintaining data collection and analysis systems in support of research protocol; may coordinate the collection and analysis of research data.
3. Prepared and reviewed documents submitted to the institutional review board (IRB).
4. Recruits, instructs, and coordinates research subjects and/or volunteers, as appropriate to specific study objectives and work scope.
5. Ensures the smooth and efficient day-to-day operation of research and data collection activities; acts as the primary administrative point of contact for internal research staff and as the principle operational liaison for other research organizations, funding agencies and regulating bodies.
6. Coordinates the day-to-day activities of any technical support staff specifically engaged in the carrying out of research/clinical protocol, as appropriate to the position; may perform aspects of research protocol, as required, in accordance with specified program objectives.
7. Plans and coordinates the staffing of research studies, to include the recruitment and administration of research support staff, as appropriate to the activity.
8. Supervises and coordinates the provision of support services to investigators and researchers.

Experience

5-7 Years

Level

Executive

Education

BS

Description :

1. Coordinate and assist with pediatric mechanism of injury identification project Coordinate data gathering from national experts on how to successfully perform prehospital clinical trials Collect, analyze, and disseminate research data.
2. Report program data and progress to study investigators.
3. Work with Principle Investigator to develop, implement, and maintain comprehensive databases and files related to the program Identify problems or obstacles in the system/procedures related to implementation of the research protocols and communicate to the study investigators Assure compliance with all relevant IRB and other regulatory agency requirements Prepare IRB documents and reports.
4. Evaluate and write research protocols in collaboration with the study investigator Collaborate on the development of program materials including educational materials, marketing materials, websites, forms, and reports Maintain program timeline including tracking deadlines for program components.
5. Coordinate program outreach activities including acting as a liaison with community organizations.
6. Organize internal and external meetings, site visits, and special events Monitor study related budgets.
7. Participate in the development of program resources through literature searches, contact with outside programs, and review of funding opportunities.

Experience

5-7 Years

Level

Executive

Education

Behavioral Health

Description :

1. Coordinated food specimen collections, transport, and documentation for projects funded by USDA/NIFA.
   
2. Conducted comprehensive literature review analysis to support faculty investigators in writing study protocols.
3. Authored reports based on study findings, and contributed to proposal designs and manuscripts.
4. Spearheaded development and completion of project reports and source documents that identified consumer handling, storage, labels, and use of product dates as risk factors for contracting food borne illnesses.
5. Internally collaborated with communications department to develop and disseminate deliverables aimed at increasing knowledge of and reducing incidence of food borne illnesses.
6. Researched differences in food safety knowledge and practices among seniors in demographic subgroups and suggested reasonable recommendations to ultimately increase seniors' knowledge of safe food handling practices, reduce risky food storage practices, and reduce food borne illnesses within the senior community.
7. Monitored and ensured IRB compliance throughout study activities.

Experience

5-7 Years

Level

Executive

Education

Doctor Of Public Health

Description :

1. Responsible for recruiting participants into several studies.
2. Responsible for conducting participant interviews with candidates who have qualified for federally funded drug and alcohol research studies.
3. Interviews consist of conducting a Form-90 and/or timeline follow-back interview, administering the SCID (Structured Clinical Interview for DSM-IV) and using a variety of assessment tools.
4. Track participants to achieve high follow-up rates, by means of phone calls, sending letters, internet searches, contacting locator's and collaterals, home visits and in some instances, jail visits.
5. Work with a diverse population in both languages (English and Spanish) and always ensure that comfort and confidentiality are preserved for each participant.
6. Plan, implement and maintain data collection and analysis systems in support of each protocol.
7. Plan and coordinate the initiation of research study protocols and the establishment of operating policies and procedures.
8. Create and design a variety of project documents to be used in a study.

Experience

2-5 Years

Level

Junior

Education

Certificate

Description :

1. Coordinated the development, initiation, set up and enrolment of patients on clinical trial protocols.
2. Coordinated the trial operations on site and at multiple participating sites Monitored trial patients' clinical status weekly on Electronic Medical Record to ensure continuing eligibility on study.
3. Collaborated with Principal Investigators to develop study protocols, tracking forms, protocol amendments, Informed Consent Forms (ICFs), Case Report Forms (CRFs) and other study related documents.
4. Ensured proper storage, dispensation, and accountability of all investigational product(s) and trial-related materials.
5. Worked closely with principal investigators on study protocols to ensure regulatory compliance.
6. Monitored the clinical trial according to company Standard Operating Procedures (SOPs) and in accordance with Good Clinical Practice (GCP).
7. Completed initial registration and continuing reporting to Institutional Review Board.
8. Tracked and reported all adverse events, protocol deviations, and other unusual activity on study.

Experience

2-5 Years

Level

Junior

Education

Public Health

Description :

1. Prepared and submitted research documents for clinical trials and worked with Institutional review board and other local and regional regulatory bodies on research compliance.
2. Screened and enrolled participants in research projects, randomized research subjects, conducted 'Informed consenting' to eligible patients and conducted research visits.
3. Organized and analyzed patients' study data.
4. Worked with on-line databases of the University of Maryland Medical Center to obtain and verify laboratory, biopsy report, imaging, culture and sensitivity test results for the purpose of research activities.
5. Conducted regulatory and compliance activities on research studies.
6. Reporting 'Serious Adverse Events' to regulatory authorities like the Institutional Review board and FDA and on potentially negative events occurring in clinical trials.
7. Coordinated with investigators and sponsors on all clinical, and regulatory matters.
8. Helped in auditing and monitoring visits by the regulatory bodies or their agents.

Experience

2-5 Years

Level

Junior

Education

Medical Education

Description :

1. Manage recruitment, screening and enrollment for NIH-funded study on maternal and child health Draft technical protocols for data collection, biological specimen collection and participant recruitment, enrollment and retention.
2. Manage data entry, database tracking and data analysis on UNIX, SAS and Microsoft Excel.
3. Manage secure storage of medical release forms and consent forms.
4. Manage budget amendments, contracts, reimbursements and invoices.
5. Designed and reviewed online and paper questionnaires and study forms for collecting prospective longitudinal data.
6. Collaborate with external study sites for maintaining accurate data and drafting reports.
7. Coordinate with external laboratory for collection, processing and storage of biological specimen from participants Coordinate with vendors for printing and mailing study forms, letters and postcards.
8. Maintain communication with IRB for approval of study protocols, study documents, securing sensitive information and annual progress reports.

Experience

5-7 Years

Level

Management

Education

MPH

Description :

1. Instruct research staff in scientific and procedural aspects of studies including standards of care, informed consent procedures, or documentation procedures.
2. Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, and discussions with physicians and nurses.
3. Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies.
4. Direct the requisition, collection, labeling, storage, or shipment of specimens.
5. Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.
6. Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.
7. Identify protocol problems, inform investigators of problems, or assist in problem resolution efforts such as protocol revisions.

Experience

7-10 Years

Level

Management

Education

Liberal Arts

Description :

1. Coordinate the daily activities of the Research department.
2. Interact with Family Support Services and recovery personnel to optimize research screening and recovery procedures.
3. Assist recovery technicians with screening and coordinating of post mortem tissue recovery.
4. Coordinate the distribution of research specimens; coordinate the receipt, delivery, and distribution of tissue specimen derivatives including archive slides and blocks.
5. Ensure tissue preparation meets AATB, FDA, and current laboratory and research standards.
6. Developed and maintained bio-specimen resource database and specimen inventory systems for all recovered SETA tissue to include fresh and frozen Research tissues, stored Bio-specimen tissues, and fresh and frozen Placenta tissue for transplant.
7. Coordinate appropriate histological services and QC functions to ensure suitability of specimens.
8. Review clinical data and make requests for additional records.

Experience

7-10 Years

Level

Management

Education

Associate In Science

Description :

1. Developed and managed social marketing campaigns, conducted outreach to minority communities, coordinated and implemented recruitment efforts and tracking of participants.
2. Created and distributed recruitment materials.
3. Resourcefully and creatively delivered facets of the project that could not be funded.
4. Coordinated and facilitated strengths-based focus groups with LGBTQ adolescents ages 13-19 throughout Washington State.
5. Presented the study to agencies across the state.
6. Collected, managed and analyzed preliminary data using SPSS statistical software.
7. Performed outreach activities to establish partnerships with other professionals and agencies, educated about the role of research within the community, and identified potential participants.
8. Practiced culturally competent research, regularly sought and implemented community feedback and advocated for changes to survey instrument based on feedback from the community.

Experience

5-7 Years

Level

Executive

Education

M.S.W. In Clinical

Description :

1. Ensured quality, consistency, and accuracy in the conduct of clinical research trials and completion of case report forms.
2. Screened potential patients and targeted specific study and enrollment goals.
3. Developed source documents for new clinical research projects.
4. Maintained accurate communication with project manager, study monitors, and related study personnel.
5. Coordinated study procedures and activities with participating co-investigators regarding ongoing and/or upcoming studies.
6. Conducted initiation meetings in conjunction with study sponsors.
7. Maintained drug accountability, protocol compliance, and FDA regulatory compliance.

Experience

2-5 Years

Level

Junior

Education

Diploma