Clinical Research Assistant Job Description
Clinical Research Assistant Duties & Responsibilities
To write an effective clinical research assistant job description, begin by listing detailed duties, responsibilities and expectations. We have included clinical research assistant job description templates that you can modify and use.
Sample responsibilities for this position include:
Clinical Research Assistant Qualifications
Qualifications for a job description may include education, certification, and experience.
Licensing or Certifications for Clinical Research Assistant
List any licenses or certifications required by the position: CITI, IRB, BLS, ACLS, HIPAA, CRS, II, IV, SOCRA, ACRP
Education for Clinical Research Assistant
Typically a job would require a certain level of education.
Employers hiring for the clinical research assistant job most commonly would prefer for their future employee to have a relevant degree such as Bachelor's and Collage Degree in Education, Computer, Medical, Health Care, Communication, Science, Health, Biology, Medicine, Faculty
Skills for Clinical Research Assistant
Desired skills for clinical research assistant include:
Desired experience for clinical research assistant includes:
Clinical Research Assistant Examples
Clinical Research Assistant Job Description
- Assist in protocol development and provide input into descriptions of routine CT research procedures
- Assist with Physiologic Imaging Research Facility development related to administrative duties including billing and scheduling
- Serves as a primary contact for clinical centers in multi-center research studies
- Develop study materials – serving to train imaging sites
- Assure study protocol compliance of CT data receipt by the Imaging Laboratory
- Screen, recruit, and obtain informed consents for clinical trials/studies
- Assist principal investigator to determine subject eligibility
- Schedule trial related procedures and visits
- Assist with subject assessments during study participation
- Assist in budget development and management of resources/supplies for study
- Knowledge of ICH/GCP guidelines required
- MUST be articulate and have excellent communication skills as much of time will be spent on the phone
- Experience with Oncology is preferred but not required
- Experience as a clinical monitor, clinical research coordinator, regulatory document specialist, or data manager is preferred
- Fluent in French, Dutch and in English, both written and verbal
- Contribute to identification of increased cost/inefficient spending and cost containment measures
Clinical Research Assistant Job Description
- Assisting the clinical team with administrative activities as required
- Assisting Clinical Manager with monitoring tasks as required
- Administer questionnaires, and assists with procedures for obtaining patient screening and recruitment obtaining research specimens
- Collects and organizes patient data, may initiates and maintain contact with study participants
- In conjunction with the PI, develops, and under the direction of project manager, assists with writing, and implementation of new research protocols including design, data collection systems and institutional review board approval (IRB)
- The Clinical Research Assistant will have the primary responsibility for assisting with the coordination of various aspects of research trials
- Interact and correspond with various internal and external constituents including sponsors, cooperative groups, Institutional Review Board and regulatory agencies
- Assisting with enrolling, registering and screening patients for clinical research trials
- Perform various administrative duties, which may include proper collection and shipment of lab samples
- Clinical trial enrollment reconciliation
- A minimum of an Associate Degree with minimum 2 years of industry experience is required or H.S
- A Bachelor’s degree preferred in science or health-care field, or equivalent
- Clinical research experience, particularly with mood disorder patients
- Minimum of 2 years of experience supporting clinical trials in a GCP environment required
- At least 6 months to 1 year of RT experience
- Must be proficient in computer software applications (Microsoft Office Suite)
Clinical Research Assistant Job Description
- Collects and records study data
- Drafting informed consents
- Collects and organizes patient data from medical records, physicians
- Provides administrative support for clinic organization and operation for the smaller subspecialty clinics
- Printing and distribution of study questionnaires by mail and/or Fax to patient providers and/or patients and speaking to subject by phone to gather clinical data
- Obtaining informed consent by phone and authorization for release of health information
- Obtain patient data from Social Security Death Master File
- Run queries from electronic database and IT department and follow up queries
- Patient data entry and maintaining research databases
- Facilitate project-related coordination and communications between investigators, IRB office, Biostatistician, or other regulatory office with PI oversight
- Typically 1-2 years of professional work experience, must include clinical research or related experience
- Certification by the American Registry of Radiologic Technologist (ARRT) in diagnostic Radiology
- The ability to learn to efficiently use existing proprietary software
- Certification by the American Registry of Radiologic Technologist (ARRT) in Computed Tomography (CT)
- College degree and one year of relevant experience or an equivalent combination of experience, education, and training
- Manual dexterity and visual acuity necessary for handling and processing specimens for testing, including preparation of specimens, operation of laboratory equipment, microscopic examination
Clinical Research Assistant Job Description
- Ensure thorough familiarity with study protocols and manual of procedures
- Participate in ongoing education in clinical research through the hospital offered programs
- Screen potential pregnant and non-pregnant subjects for study eligibility
- Serve as the primary study contact for subjects/potential subjects prior to enrollment and throughout the duration of the study
- Coordinate initial and follow-up study visits
- Initiates and maintains contact with study participants
- In conjunction with Principal Investigators, develops and implements new research protocols, institutional review board applications (IRB), and grant applications
- Assists PIs with literature searches, preparation of slide presentations, poster presentations, and written published articles, as required
- Performs all other miscellaneous research and administrative duties as assigned
- The Clinical Research Assistant will provide support for clinical trials and research conducted in the Department of Emergency Medicine
- Have the ability to use the internet and other computer programs, , database applications
- Formal Cover Letter
- Unofficial Transcripts from all Universities Attended
- Must possess integrity to maintain confidentiality
- Ability to work effectively in a fast-paced, team-based environment
- Experience working with clinical data to improve processes of care
Clinical Research Assistant Job Description
- Screen, consent and enroll patients in ED research studies
- Working with research nurses, manage research databases for industry sponsored and investigator initiated studies
- Coordinate pick up/transport of research samples
- Assist research nurses with progress reports for industry sponsored clinical trials
- Manage IRB accounts for multiple studies
- Consults with and assists staff in own and other labs in conducting research projects
- Performs data entry and manages study database as directed and performs other administrative duties related to the study as assigned
- Record readings in Excel while Pathologist reviews slides
- Pull approximately 5000 samples from freezer and record data
- Problem solve location of slides in multiple freezers
- Capable of interacting pleasantly and positively with others
- Possess knowledge of position requirements
- Skill in working with clinical and/or psychiatric research procedures
- Knowledge of best practices in field familiarity with relevant federal, state and other regulatory requirements
- Undergraduate research experience, preferably with human participants (not just lab setting)
- MUST be articulate and have clear/concise communication skills