Research Coordinator Resume Samples

A Research Coordinator works under a Clinical Research Manager and is tasked with the duty of administering clinical trials. The primary responsibilities listed on the Research Coordinator Resume include the following – managing clinical trials, collecting data, administering questionnaires; overseeing the running of clinical trials; managing research budgets; administering questionnaires; adhering to ethical standards; collecting and analyzing data obtained through research, and ensuring that necessary supplies and equipment are stocked. The job duty also includes liaising with laboratories in findings; and participating actively in subject recruitment efforts.

To undertake the above-mentioned duties, the following skills are required – nursing expertise, analytical mindset, exceptional interpersonal skills, and outstanding written and verbal communication skills; the ability to adhere to ethical standards; familiarity with research regulatory standards; and passion for self-education. A Degree or an associate’s degree in nursing or related field is required.

Research Coordinator Resume

Objective : Seeking to expand my scientific knowledge in a growing field of medical science. As a Research Coordinator, I discovered a strong interest and strength in developing and applying new technologies to advance the clinical research process.

Skills : Excel, Word, Community Outreach, Community Relations, Public Speaking, Professional Presentations, Written Communication, Community Engagement.

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.
Years of Experience
Experience
2-5 Years
Experience Level
Level
Executive
Education
Education
Public Health


Clinical Research Coordinator Resume

Headline : Seeking a Clinical Research Coordinator or related position in the field of Clinical Research Study.

Skills : Microsoft Office, Carpentry, Circuitry, masonry, Solidworks 2013.

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.
Years of Experience
Experience
5-7 Years
Experience Level
Level
Executive
Education
Education
BS


Sr. Research Coordinator Resume

Headline : Seeking to transition to a career in the veterinary field. Extensive experience assisting with veterinary procedures and handling animals through volunteer work with the Society and City Wildlife.

Skills : Health education; Program design; Quantitative data analysis; Qualitative data analysis; Employee training; Health promotion; Project Management; Program evaluation; Motivational interviewing.

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.
Years of Experience
Experience
5-7 Years
Experience Level
Level
Executive
Education
Education
Behavioral Health

Jr. Research Coordinator Resume

Headline : Service-oriented technician with 10-year background in pharmacy. Core competencies include customer service, quality control, and data entry as well as excellent communication and time management skills. Handles tasks with accuracy and efficiency.

Skills : Basic Biomedical and Clinical Research, Medical Terminology,.

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.
Years of Experience
Experience
5-7 Years
Experience Level
Level
Executive
Education
Education
Doctor Of Public Health

Research Coordinator III Resume

Objective : Committed to deliver high quality results with little to no supervision. Dedicated and focused at prioritizing and completing multiple tasks simultaneously. Bilingual/Bicultural. Familiar with Microsoft Office applications.

Skills : Microsoft, Yardi Genesis, CNA.

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.
Years of Experience
Experience
2-5 Years
Experience Level
Level
Junior
Education
Education
Certificate

Research Coordinator II Resume

Objective : To secure a position in clinical research using my knowledge of medicine, project management and comprehensive understanding of the clinical operations process.

Skills : R, SAS, Matlab, Data Analysis, Data Mining, C.

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.
Years of Experience
Experience
2-5 Years
Experience Level
Level
Junior
Education
Education
Public Health

Research Coordinator I Resume

Objective : Skilled Clinical researcher, experienced in running and coordinating clinical trials, case-control studies, performing epidemiological and statistical analysis, overseeing research compliance activities, managing health programs, writing of scientific papers and conducting teaching sessions, work-shops and seminars.

Skills : Research, Program Management.

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.
Years of Experience
Experience
2-5 Years
Experience Level
Level
Junior
Education
Education
Medical Education

Research Coordinator/Analyst Resume

Headline : Currently working towards a certificate in Geospatial science, Constantly growing and applying my skills using ArcGIS. In an academic setting, I have experience performing analyses on geographic information using the the spatial analyst tool and manipulating raster images. Professionally, extensive experience georeferencing map images and digitizing the spatial information.

Skills : Microsoft Office Suite, SAS Stasticial Programming, Project Management, Literature Reviews, Medical Terminology, UNIX, REDCap.

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.
Years of Experience
Experience
5-7 Years
Experience Level
Level
Management
Education
Education
MPH

Research Coordinator/Supervisor Resume

Summary : Ability to work well on a team and independently Bachelor's Degree with relevant healthcare, business, and science courses. Highly organized and motivated with great attention to detail.

Skills : Pharmacogenomic Research, Assistant Nursing, Office Assisting, Teaching.

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.
Years of Experience
Experience
7-10 Years
Experience Level
Level
Management
Education
Education
Liberal Arts

Research Coordinator/Manager Resume

Summary : To utilize the skills, education, organization, and leadership abilities I have gleaned in the U.S. Air Force, Tissue Banking, and medical industry to help support a company focused on enhancing the lives and safety of others.

Skills : Photography, Data Management, Data Entry, Administrative Support, Microsoft Office, Volunteer Management.

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.
Years of Experience
Experience
7-10 Years
Experience Level
Level
Management
Education
Education
Associate In Science

Associate Research Coordinator Resume

Headline : Over 20 years experience in research and laboratory setting, acute care, short and long term care and rehabilitation setting is seeking a full time research related position (data manager, site monitor, etc.).

Skills : Social Work, Mental Health Specialist, Creative Writing, Academic Research, Marketing And Sales, Community Development.

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.
Years of Experience
Experience
5-7 Years
Experience Level
Level
Executive
Education
Education
M.S.W. In Clinical

Research Coordinator Resume

Objective : One year clinical research coordinator experience Near 10 years research experience as a research associate. With solid background and extensive experience in the field of neuroscience, molecular biology, cell biology, gene expression and nutrition. Supervised graduate students, technical demonstration as well as trouble shooting. Self-motivated with the ability to work effectively within a collaborative environment as well as independently.

Skills : Interpersonal communications, research, IRB, regulatory compliance, protected populations experience, research, data managment, Microsoft Office, administration, team building, image processing, data analysis MRI, EEG.

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.
Years of Experience
Experience
2-5 Years
Experience Level
Level
Junior
Education
Education
Diploma