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 : With a robust background in clinical research spanning over five years, I bring a proven ability to manage complex studies while ensuring compliance with regulatory standards. My experience encompasses patient recruitment, data management, and adherence to Good Clinical Practices (GCP), which has enhanced the integrity of research outcomes. I am eager to leverage my analytical skills and collaborative approach to contribute effectively as a Clinical Research Intern.
Skills : Data Management Software, Regulatory Compliance, Patient Recruitment, Data Analysis
Description :
Served as Clinical Research Coordinator for a Transcranial Direct Current Stimulation study, overseeing participant recruitment and data collection.
Directed the recruitment process for cognitive remediation studies, ensuring compliance with ethical standards.
Reviewed and validated medical source documents for accuracy and completeness.
Participated in project review meetings to ensure alignment with research objectives.
Conducted patient interviews, assessing both positive and negative symptoms to support clinical evaluations.
Administered baseline and endpoint assessments, contributing to the overall study efficacy.
Managed and updated the research database, ensuring data integrity and accessibility.
Experience
2-5 Years
Level
Executive
Education
B.S. Biology
Clinical Research Intern Resume
Objective : Possessing a solid five-year foundation in clinical research, I excel in orchestrating multifaceted studies while upholding rigorous compliance with industry regulations. My expertise includes participant recruitment, meticulous data management, and strict adherence to Good Clinical Practices (GCP), significantly contributing to the reliability of research findings. I am committed to applying my analytical capabilities and teamwork skills to drive impactful contributions as a Clinical Research Intern.
Skills : Clinical Research Knowledge, Data Management Proficiency, Statistical Analysis Software Proficiency, Presentation Skills, Adaptability and Flexibility
Description :
Executed patient visit schedules in strict accordance with study protocols.
Managed Electronic Case Report Forms (eCRF) using Phase Forward and Medidata Rave systems.
Conducted study-related procedures while ensuring compliance with protocols, GCP, and regulatory standards.
Monitored and organized clinical data flow, addressing queries promptly to maintain data integrity.
Supported team members with administrative tasks crucial for the execution of clinical trials.
Assisted in periodic reviews of study documentation to ensure accuracy and completeness.
Experience
2-5 Years
Level
Executive
Education
B.S. Biology
Clinical Research Intern Resume
Objective : A motivated and detail-oriented individual with two years of clinical research experience, specializing in patient engagement and data integrity. I possess hands-on expertise in conducting clinical assessments, managing data entry, and ensuring compliance with Good Clinical Practices (GCP). My strong analytical abilities and effective communication skills empower me to contribute meaningfully to research projects and enhance participant safety.
Skills : Clinical Trial, Clinical Research Methodologies, Good Clinical Practices (GCP), Data Analysis Software, Data Collection Techniques
Description :
Supported Clinical Research Coordinators with patient visits, documentation, CRF completion, and data queries during monitor visits.
Executed clinical tasks as per study protocols, including phlebotomy, blood pressure monitoring, and other necessary procedures.
Assisted with laboratory duties, including quality assurance reviews and specimen processing.
Conducted consult visits and maintained accurate patient records, ensuring data integrity.
Facilitated the creation and organization of patient files for study closeout, ensuring compliance with regulatory requirements.
Performed data entry and updates in patient databases to enhance research accuracy.
Participated in the preparation of study documentation, including memos and progress notes.
Experience
0-2 Years
Level
Entry Level
Education
BS Biology
Clinical Research Intern Resume
Objective : Bringing over five years of diverse experience in clinical research, I have effectively contributed to the advancement of medical studies through rigorous adherence to regulatory standards and ethical practices. My comprehensive background includes expertise in patient recruitment, data analysis, and protocol adherence, ensuring high-quality research outcomes.
Skills : Data Analysis and Interpretation, Patient Recruitment Strategies, Regulatory Compliance, Good Clinical Practice (GCP)
Description :
Conducted comprehensive literature reviews and research to support ongoing clinical studies in immunology.
Executed enzyme-linked immunosorbent assays (ELISAs) for accurate detection of biomarkers in pediatric patients.
Registered as an EMT with BLS certification, enhancing emergency response capabilities during clinical trials.
Coordinated multiple clinical trials focused on weight loss, hypertension, and prostate cancer, ensuring compliance with IRB and GCP guidelines.
Assisted in drafting protocol manuals detailing recruitment strategies, informed consent processes, and data collection methods.
Monitored trial activities to ensure adherence to protocols, providing timely updates and recommendations to the research team.
Organized and maintained study-related documentation, enhancing the efficiency of record-keeping processes.
Experience
2-5 Years
Level
Executive
Education
B.S. Biology
Clinical Research Intern Resume
Objective : As a dedicated clinical research professional with over five years of experience, I possess a strong track record in executing and overseeing clinical trials while ensuring adherence to rigorous compliance standards. My expertise encompasses patient recruitment, data integrity, and thorough understanding of regulatory requirements, including Good Clinical Practices (GCP). I am enthusiastic about utilizing my analytical skills and collaborative mindset to make significant contributions as a Clinical Research Intern.
Skills : Clinical Data Management, Statistical Analysis, Clinical Trial Design, Data Querying and Reporting, Data Visualization Techniques
Description :
Entered, analyzed, and interpreted qualitative and quantitative data for clinical trials, ensuring data accuracy and compliance.
Conducted research on the efficacy of interventions for breast cancer survivors, demonstrating the impact on quality of life.
Facilitated the informed consent process, ensuring participant understanding and compliance.
Reviewed and updated Electronic Case Report Forms (ECRF) to maintain data integrity.
Assisted in organizing and maintaining essential regulatory documents for audits and inspections.
Coordinated logistics for clinical trials, including the management of supplies and equipment.
Objective : Driven by a passion for advancing clinical research, I have accumulated over five years of experience in managing diverse research studies and ensuring compliance with ethical standards. My background includes extensive involvement in patient recruitment, data integrity, and regulatory adherence, which has significantly bolstered the quality of study outcomes. I am poised to apply my analytical expertise and collaborative spirit to make substantial contributions as a Clinical Research Intern.
Skills : Clinical Data Analysis, Clinical Trial Management, Statistical Software Proficiency, Data Visualization Tools
Description :
Led a Phase II Clinical Trial for Amyotrophic Lateral Sclerosis, ensuring compliance with regulatory guidelines.
Managed both paper and electronic Trial Master Files (TMF) for a large multi-center study.
Collaborated with clinical project teams across various studies and therapeutic areas, enhancing operational efficiency.
Developed and maintained project task checklists for in-house and regional Clinical Research Associates (CRA).
Tracked and reported metrics related to IRB approvals, safety correspondence, and adverse events.
Documented and summarized meeting minutes for weekly CRA and CRO sponsor team meetings.
Assisted in recruiting, consenting, and interviewing patients for multi-site clinical assessments, ensuring ethical standards were met.
Experience
2-5 Years
Level
Executive
Education
B.S. Biology
Clinical Research Intern Resume
Objective : As an accomplished clinical research professional with five years of extensive experience, I have honed my ability to drive innovative research initiatives while maintaining strict adherence to ethical standards and regulatory compliance. My background includes a strong focus on patient engagement, data integrity, and the application of advanced research methodologies, which have consistently enhanced the quality of clinical outcomes. I am eager to apply my strategic insights and collaborative approach to make valuable contributions as a Clinical Research Intern.
Skills : Proficient in Microsoft Word, Advanced Excel Skills, Expertise in PowerPoint Presentation, Familiarity with Connexus Software, Fundamental Laboratory Techniques in Biology and Chemistry
Description :
Administered cognitive assessments to evaluate patient eligibility and cognitive function in clinical trials.
Facilitated communication with study participants, addressing inquiries and providing essential information about the research process.
Generated comprehensive reports and documentation to support research findings and maintain regulatory compliance.
Applied statistical analysis to interpret data trends and inform research decisions.
Conducted literature reviews to support the development of research protocols and study designs.
Organized and maintained study documentation, ensuring accuracy and timely filing in compliance with regulatory standards.
Collaborated with interdisciplinary teams to enhance the efficiency of clinical trial operations.
Experience
2-5 Years
Level
Executive
Education
B.S. Biology
Clinical Research Intern Resume
Objective : Aspiring Clinical Research Intern with two years of hands-on experience in clinical trials, focusing on patient recruitment and data collection. Skilled in ensuring compliance with Good Clinical Practices (GCP) and maintaining meticulous records to support research integrity. I am committed to advancing healthcare through rigorous research methodologies and collaborative teamwork.
Skills : Microsoft Office Suite, Cross-Platform Software Proficiency, Professional Networking Skills, Clinical Data Management, Regulatory Compliance Knowledge
Description :
Conducted interviews with study participants to gather essential information for clinical trials.
Collaborated with various departments to facilitate data sharing and enhance research efficiency.
Reviewed trial data for accuracy and completeness, adhering to established protocols.
Drafted and maintained communication documents, including emails and memos, to ensure clarity among team members.
Documented clinical trial data meticulously to support regulatory compliance and research integrity.
Demonstrated a solid understanding of clinical research protocols and ethical guidelines.
Utilized data management systems to organize and maintain participant records effectively.
Experience
0-2 Years
Level
Entry Level
Education
B.S. in Biology
Clinical Research Intern Resume
Objective : Equipped with over five years of comprehensive clinical research experience, I have successfully managed and executed numerous studies, ensuring strict adherence to regulatory standards and ethical guidelines. My expertise includes participant recruitment, data analysis, and maintaining compliance with Good Clinical Practices (GCP), all of which have significantly enhanced the quality of research outcomes. I am motivated to utilize my analytical skills and collaborative mindset to drive impactful contributions as a Clinical Research Intern.
Ensured compliance with funding and regulatory guidelines throughout clinical research projects.
Maintained up-to-date knowledge of human research protection protocols and relevant best practices.
Completed IRB submissions accurately and on schedule, facilitating timely project initiation.
Proactively identified study needs and executed tasks effectively to meet deadlines.
Collaborated with team members and sought assistance when necessary to enhance project outcomes.
Collected and analyzed data to support operational and clinical research activities.
Entered clinical and research data into electronic systems, including CRFs and tracking databases.
Experience
2-5 Years
Level
Executive
Education
B.S. Biology
Clinical Research Intern Resume
Objective : Motivated Clinical Research Intern skilled in patient recruitment and data management. Successfully supported a team in executing clinical trials, leading to a 15% increase in participant enrollment and streamlined data reporting processes.
Skills : Clinical Trial Planning, Patient Recruitment, Data Analysis, Good Clinical Practices (GCP), Data Integrity
Description :
Adhered to established protocols in the collection of clinical data and administration of clinical studies.
Supported aggregation and analysis of study data under the guidance of senior research staff.
Participated actively in team meetings, collaborating to set and achieve project timelines and deliverables.
Completed necessary training and certification as mandated by study protocols, including CITI training.
Fulfilled all study requirements such as CHEX and Human Subjects training as required.
Maintained comprehensive records and reference materials essential for departmental operations.
Conducted quality checks to ensure compliance with study protocols and data integrity.
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