Clinical research associates manage ongoing clinical research projects. Their duties include keeping records of ongoing protocols, conducting literature searches for new information, developing and refining methods and procedures to aid in the efficiency and accuracy of research work, updating electronic case report forms to record study data, and reviewing accessioning documentation for quality control. Clinical research associates must have a bachelor’s degree in biology or a related field along with 2-3 years of experience in lab management. They should be detail-oriented team players who are resourceful, organized, motivated self-starters, and able to learn quickly.
A good resume is well-written and concise. It should be neat and easy to read, listing previous experience in a logical order.
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Contents
The Best Clinical Research Associate Resume Samples
These are some examples of accomplishments we have handpicked from real Clinical Research Associate resumes for your reference.
Clinical Research Associate
- Setting up the trial sites, which includes ensuring each center has the trial materials, including the investigational medicinal product.
- Identifying and assessing the suitability of facilities to be used as the clinical trial site.
- Identifying/selecting investigators who will be responsible for the conduct of the trial at the trial site.
- Organize and make presentations at trial sites in regards to trial-specific industry standards.
- Provide support and guidance to women in their transition into the world of breast cancer research.
Clinical Research Associate
- Responsible for remote centralized monitoring as the 1 line of contact for site support and management of assigned projects.
- Maintain regular phone and email contact with assigned sites for duration of study activities and maintain communication logs.
- Maintain flexible phone and travel availability to accommodate communication with organizations and sites globally.
- Knowledge is current and in accordance with standards of procedure and work practices; IRB, GCP, and ICH guidelines.
- Initiate developing a comprehensive program to aid in new mothers’ breastfeeding skills and motivation.
Clinical Research Associate
- Provided regulatory consultation and training services to investigators and research staff on the application and implementation of the federal regulations, state laws, and institutional policies for human subjects research.
- Review research project applications and documents to ensure researchers comply with regulatory and ethical laws for the protection of human subjects.
- Communicate with sponsors to ensure completeness and accuracy of study documents for IRB submission and study initiation.
- Developed a research proposal to examine socializing and alcohol use among college students, Social Psychology course by major.
- Authored re-write of journal article proposal.
Clinical Research Associate
- Conduct all level of monitoring visits in accordance to GCPs and applicable local and international regulations and SOPs.
- This encompasses clinical trial material, accountability, regulatory document review and submission, clear and complete trip report writing and site management.
- Track and maintain site visits calendars, Transmittal logs, Training logs and contact list as appropriate.
- Verify patient eligibility, communicate and document protocol deviations and non-compliance.
- Researched craft project guidelines for use in computer science class, Advanced Programming.
Clinical Research Associate
- Assisting in the oversight of the clinical study conduct, including protocol and CRF development, investigator brochures, ICFs, reports and publications, per all applicable regulations and company Standard Operating Procedures.
- Reviewing clinical trial data in accordance with [Global] Data Management Plans and applicable standardized data management processes (SOPs, Work Instructions, etc.) to identify erroneous, missing, incomplete, or implausible data.
- Assisting with the reconciliation of central laboratory and third party vendor data (eCRF, eDiary, specialty laboratory, etc.).
- Assisted in analyzing and recording patient data.
- Evaluated results in furtherance of patient care, research, and databases development.
Clinical Research Associate
- Clinical trial preparation involving the planning, assembling and instruction of the trial team, development and evaluation of patient information and informed consent forms and patient recruitment.
- Regulatory and ethical submissions and procedures and communicating with relevant authorities.
- CRA Implementation of the clinical trial from initiation through the stages of development documents, SOPs, tools, organization facilities and licenses.
- Performed and document pre-study site evaluations, site initiations, regulatory document collection, interim monitoring and study close out visits in accordance with GCP, study-specific requirements, clinical monitoring plans, company SOPs, applicable regulatory requirements and defined quality and performance standards.
- Used statistical analysis to determine response rate per study protocol; supervised graduate student employees.
Clinical Research Associate
- Liaise with principal investigators and research techs, research monitoring for multi site oncology studies, managing supplies, patient / subject coordination, generate and manage budgets, asses risks and benefits, adverse event recording and documentation.
- Deliver presentations to key opinion leaders on use of PET CT for primary care and research, research data collection, research monitoring, and marketing strategies for medical imaging services and oncology research. Perform quality assurance / control, manage and oversee clinical services.
- Serve as the Radiation Safety Officer for imaging center to ensure strict adherence with all Federal and State regulations.
- Applied clinical research experience towards mastery of complex medical terminology, procedural protocols, pharmaceutical formularies, and transferable knowledge into organizational standard operating procedures.
- Gained new knowledge of the power of research, evidence-based decision-making, and extensive knowledge of the health care system as a result of conducting clinical research.
Clinical Research Associate
- Assisted with the development and execution of clinical research studies and programs.
- Worked under specific instructions to assist with routine tests, experiments, and procedures.
- Collected, processed, and assisted in the compilation and verification of research data, samples/specimens (following strict protocol and detailed instructions).
- Entered data from forms and documents into databases and other documents.
- Assisted with routine data verification and quality control, ensuring data integrity and • consistency with prescribed study protocol.
Clinical Research Associate
- Managed assigned investigational study sites and perform on-site quality reviews of Case Report Form data.
- Ensure investigative sites are in compliance with protocol, FDA regulations and ICH/GCP guidelines and company standard operating procedure.
- Review Investigator Site File notebook for completeness and up-to-date information including IRB- related documents.
- Achieved additional knowledge of study design and methods for research designs through coursework in medical statistics.
- Fabricated literature reviews on topics reviewed by peers for their professional interests.
Clinical Research Associate
- Provided monitoring, planning, organization, communication and implementation of study objectives for assigned protocol(s) as a lead member of the team.
- Performed management of study site activities to ensure the integrity of clinical data, in adherence to all applicable regulations, Good Clinical Practices, Standard Operating Procedures (SOPs), and Project Specific Operating Procedures (PSOPs).
- Assumed the role of a Lead CRA on projects by providing direction and guidance to project team, coordinating all monitoring activities, and communicating the status of these activities to the study Project Leader.
- Developed posters and presented findings from a patient satisfaction survey to the CEO, Corporate Research opening; made recommendations for further information collection.
- Completed time-critical tasks regarding the establishment and organization of a consent form in order to meet clinical trial sponsor requirements on time.
Clinical Research Associate
- Efficiently work with clinical staff including physician investigators and support staff to identify and screen possible study participants
- Documentation of patient history, casting and splinting, assisting provider with procedures and exams.
- Follow protocol based data collection procedures and follow-up schedule, maintain appropriate records and audit trail.
- Interact with sponsor in study related communication, monitoring visits and research support staff.
- Advanced research goals with data collection and analysis of clinical studies.
Clinical Research Associate
- Acted as associate auditor in many clinical site audits across the country to identify major and minor deficiencies according to GCP guidelines in order to preserve participant safety and data integrity in multiple Type 1 Diabetes trials.
- Created and maintained a database to track almost 200 mechanistic studies from applications and reviews through sample dispensation, progress reporting and study closing.
- Used the database as a template to created requirements and maintain data for the TrialNet Ancillary Study Database webpage.
- Applied statistical methods to analyze and summarize data from multi-site, multi-national clinical studies to ensure adherence to ICH ethical guidelines.
- Completed study of diabetic retinopathy treatments in less than one year; recognized by National Institute for the Blind for outstanding research.
Wrap Up
You need to make sure your resume stands out amongst the other candidates. It is the first impression that employers have of your work experience and skills. Use the samples above to put together a resume that best suits your needs and helps you get the job you want.