A Clinical Research Intern is an entry-level professional who gains practical experience in clinical research by completing a variety of research duties. Roles and responsibilities associated with the post are listed on the Clinical Research Intern Resume as – assisting the research staff, updating database, researching and noting down important concepts, helping with information management, drafting documents, completing other tasks as needed by the supervisors, and completing all other lab duties as required.
Eligible example resumes for this role showcase abilities like – research skills, the ability to follow instructions, laboratory experience, experience in conducting scientific experiments, excellent research and presentation skills, knowledge of statistics, and fluency in using relevant software. Most of the Clinical Research Interns are a final year or fresh graduates in the field of biology, microbiology, or biological sciences.
Objective : Clinical Research Intern with 3+ years of experience in Working on problems of moderate scope that require analysis and evaluation of identifiable factors and interpretation of the situation, Exercising judgment within defined and existing practices to determine specific work methods for obtaining results.
Skills : Microsoft Office, Good Clinical Practice, Electric Data Capture.
Description :
Worked as Clinical Research coordinator in Transcranial direct-current stimulation (tDCS) study for treatment-refractory auditory hallucination.
Directed the patient/subject recruitment for Transcranial Direct Current Stimulation study and Cognitive Remediation Study.
Reviewed medical source documents.
Participated in project review meeting.
Interviewed the patients and assessing their positive/negative symptoms.
Administered baseline and endpoint assessment with patients.
Managed database.
Experience
2-5 Years
Level
Executive
Education
GED
Clinical Research Intern Resume
Objective : Responsible for Contacting involve obtaining or providing information requiring little explanation or interpretation, Contributing to business and departmental functions to achieve goals and acquire work experience.
Skills : Data And Statistical Analysis, Life Science Background, Computer Proficient ,Microsoft Office Proficiency ,PowerPoint Knowledge ,Quick Learner ,Excellent Communication , Level-headed And Calm, Able To Work Efficiently In Stress Situations, A Very Strong Team Player.
Description :
Coordinated with doctors in patient handling- screening,randomization, patient follow up.
Performed the patient visit schedules as per protocol.
Handled Electronic CRF ( Phase forward and Medidata Rave) and Paper CRF.
Conducted study related procedure in compliance with protocol, GCP and regulatory guidelines.
Monitored and oversaw of queries and clinical data flow organization-wide.
Carried out assigned administrative tasks to effectively support team members with clinical trial execution.
Provided assistance with the periodic review of study files for accuracy and completeness.
Experience
2-5 Years
Level
Executive
Education
MS
Clinical Research Intern Resume
Objective : Responsible for Providing assessment and treatment of communication and swallowing disorders for both adult and pediatric populations. Administers diagnostic tests and implements appropriate treatments.
Assisted Clinical Research Coordinators with patient visits, documentation, CRF completion, data queries and monitor visits.
Performed clinical requirements of study protocols, i.e., lab work (phlebotomy and processing), blood pressure, electrocardiograms, pulmonary function testing, urine/serum pregnancy testing, strep throat screening, or any procedure necessary for the protocol as ordered by the investigator or coordinator.
Assisted in the laboratory or with other laboratory duties such as performing quality assurance review, restocking of supplies and processing of specimens.
Performed consult visits as needed.
Helped maintain accuracy with the patient database, including data entry and updating existing patient files.
Assisted the Clinical Research Coordinator or other staff members with creating and copying patient files for study closeout procedures.
Typed memos, letters, phone screeners, progress notes and various documents.
Experience
0-2 Years
Level
Entry Level
Education
GED
Clinical Research Intern Resume
Objective : Responsible for using basic office software programs, information systems, and office equipment to access, input, and verify standard information. Communicating information clearly to staff, clients, and/or public about services, processes, and procedures using prescribed or established guidelines. Utilizing program specific terminology.
Skills : Clinical Assessment, Case Management, Patient Navigation.
Description :
Researched advanced methods of UCI immunology methods in pediatrics.
Ran enzyme-linked immunosorbent assays to identify substances in lab tests.
Registered EMT with BLS.
Assigned to work on multiple clinical trials involving a weight loss study, hypertension study, and a low carbohydrate and prostate cancer study Prepared and reviewed required records of study activity for the Institutional Review Board (IRB) submission material while being compliant with GCP and ICH guidelines.
Assisted with protocol manuals that describe all procedures, research subject recruitment, participation in the informed consent process, scheduling and monitoring of study visits, data collection including participant measures and administration of study questionnaires, as well as data entry.
Monitored study activities to ensure compliance with protocols and provided study status updates to team members, including interaction to resolve facilitate project timelines.
Filed labs and correspondence.
Experience
2-5 Years
Level
Executive
Education
BA
Clinical Research Intern Resume
Objective : Clinical Research Intern with 5+ years of experience in Adhering to Occupational Safety and Health Administration (OSHA), Good Clinical Practices (GCP), Good Laboratory Practices (GLP), infection control procedures, and rules and regulations pertaining to the research site.
Entered, analyzed, and interpreted qualitative and quantitative data for the clinical trial.
Conducted my own research using the clinical trial data on the efficacy of improving quality of life in breast cancer survivors undergoing weight loss intervention programs.
Observed and participated in the informed consent process.
Reviewed and helped to update the ECRF data.
Assisted in organizing regulatory documents.
Performed various errands to pick up dry ice, supplies, samples, physician signatures and storage boxes, etc.
Ran tDCS sessions and Cognitive Remediation Therapy (CRT) group.
Experience
2-5 Years
Level
Executive
Education
GED
Clinical Research Intern Resume
Objective : Clinical Research Intern with 6 years of experience in Assisting with administrative logistics including consenting research participants, data collection, and scheduling Executes, maintains research study to include data collection.
Skills : Medical Writing, Research, Inventory Management, Adobe, Microsoft Applications, Data Management.
Maintained TMF, paper and electronic, for large multi-center study.
Assisted clinical project teams across multiple studies and therapeutic indications.
Provided in-house and regional CRA weekly project task checklist.
Tracked metrics for IRB approvals, safety correspondence, central lab data, CRFs, Monitor Reports, Site Logs, Protocol Deviations, queries, Adverse and Serious Adverse Events.
Recorded and summarized minutes for weekly CRA and CRO/Sponsor team meetings.
Peterson Recruited, consented, and interviewed patients for research projects Enrolling patients in Multi-Site Clinical Assessment of ME/CFS- Year 2 study for CDC- compiled and sent out saliva sample kits to assess Cortisol levels (Publication Pending) Aliquot spinal fluid samples and cataloged them to use in Spinal Fluid study with Dr.
Experience
2-5 Years
Level
Executive
Education
Diploma
Clinical Research Intern Resume
Objective : Responsible for Preparing research subjects (animal or human) for research study, Managing study documentation to include accurate and timely filing, Compling with all the rules and regulations as applicable to assigned duty station.
Skills : Knowledge Of Microsoft Word, Excel, Power Point, Connexus, Basic Biology And Chemistry Laboratory Techniques, PCR, Gel Electrophoresis.
Description :
Administered Matrics Consensus Cognitive Battery assessment with patients.
Answered and maked phone calls, responds to program related questions, and sends written material as appropriate.
Composed, typed, and printed reports, general letters, spreadsheets, e-mail, and memoranda from rough drafts or general instructions, involving the assembly of data from computer and paper file or record sources.
Applied research techniques and analytical methods to the study of administrative systems, organizational structures, policies, and procedures.
Conducted special studies in conjunction with a project, analyzes data and makes recommendations based upon studies.
Gathered and organized data to provide information for departmental special projects or reports, basic arithmetic computations.
Assisted in preparing written reports; accompany professional level employees on assignments.
Experience
2-5 Years
Level
Executive
Education
GED
Clinical Research Intern Resume
Objective : Seeking an entry level Clinical Research Intern position in your organization which will require me to develop my practical experience, at the same time providing excellent healthcare to patients.
Skills : Microsoft office, MAC/PC applications, Networking, Data analysis.
Description :
Conducted interviews with clients or internal personnel to obtain basic information for departmental use.
Contacted other departments or outside agencies to request or give information and other related duties as assigned.
Reviewed data and information for completeness and accuracy using standard guidelines; performs tasks with attention to detail.
Gathered readily available information from office records to drafts e-mails, memos and other documents.
Recorded and documented information accurately.
Demonstrated basic understanding of the area of specialization, of program procedures, methods, and practices to include knowledge of program and staff responsibilities.
Used established filing and data systems, functions, and/or procedures that require knowledge of the program.
Experience
0-2 Years
Level
Entry Level
Education
Certificate In Clinical Research
Clinical Research Intern Resume
Objective : Dedicated and Self-motivated professional with 2+ years clinical research experience, duties performed according to protocol, Sponsor and ICH-GCP guidelines.
Skills : Microsoft Office, PRISM Data Analysis, Image J Technique.
Description :
Ensured compliance with program guidelines and requirements of funding and regulatory agencies.
Stayed informed of and adhere to human research protection guidelines, relevant best practices, and changes to any research protocol.
Accurately completed IRB submissions on time.
An anticipated study needs and work to accomplish them in a timely manner.
Sought assistance, when needed.
Collected data in order to facilitate operational and clinical research activities.
Entered clinical and research data and information into database, include electronic CRFs and sample tracking databases.
Experience
2-5 Years
Level
Executive
Education
GED
Clinical Research Intern Resume
Objective : Clinical Research Intern with 2+ years of experience in Interacting and communicating effectively with study and site personnel, research participants, The Geneva Foundation and the study sponsor, Promoting safety and confidentiality of research participants at all times.
Skills : Planning Skills, Administrative Skills.
Description :
Followed established guidelines in the collection of clinical data and/or administration of clinical studies.
Supported aggregation and analysis of study data, as directed by senior research staff.
Attended and contributed to team meetings, including working to set and achieve project timelines and deliverables.
Obtained training and certification as required by study protocol (e.g., CITI training).
Completed all study requirements such as CHEX and Human Subjects training as required.
Complied with all annual job-related training requirements.
Analyzed, generated, and maintained records and other reference material necessary for departmental use.
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