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Clinical Research Assistant - Admin
Company | The IMA Group |
Address | Las Vegas, NV, United States |
Employment type | FULL_TIME |
Salary | |
Category | Hospitals and Health Care |
Expires | 2023-06-04 |
Posted at | 1 year ago |
Description
- Establish a working relationship with the Clinical Research Team and other personnel.
- Schedule study participants for upcoming study visits per protocol requirements.
- Perform collection of data requirements including but not limited to vital signs, EKGs, subject weights, patient diary review, subject interviews.
- Processing and shipping of lab specimens collected per protocol and laboratory manual requirements
- Prepare source documentation templates for upcoming subject visits.
- Support the regulatory submission and ongoing review process, ensuring that all documentation is up to date including screening/enrollment logs.
- Support study coordinators with administrative visit management and assistance with visit tasks as delegated.
- Patient medical record retrieval and review as needed.
- Data Entry or transcription of study visit information/assessments into both Clinical Trial Management System CTMS and a secure study specific electronic data capture systems databases EDC as authorized.
- Apply and adhere to Company Policies and SOPs, HIPAA and OSHA requirements and processes that allow for the delivery of quality services to internal and external customers.
- Answering and triage of research office calls.
- Team player - Effective participant as a team member and can demonstrate significant positive participation on successful teams.
- Must have strong communication skills, speak, and listen respectfully with the public, physicians, and co-workers.
- At least 6 months of past medical office experience, medical certificate, or equivalent previous work experience required.
- Able to adapt to a changing environment and demonstrates a make it happen attitude.
- Strong follow through skills and ability to proactively identify and solve problems; demonstrated initiative is imperative.
- Exhibits professionalism in negotiating sensitive issues.
- Must be proficient in Microsoft Office Word and Excel, CRIO - preferred, will train - and databases used in research environment.
- Possess the ability to work well under pressure, multi-task, and manage deadlines.
- Additional duties/responsibilities may be assigned as needed.
- Excellent follow-up.
- Ability to prioritize and work on multiple projects at a time
- Clinical Research or Medical Experience preferred
- High School, GED required
- Bachelors degree preferred
- Additional languages encouraged
- Familiarity with medical terminology
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