"Clinical Research Technician"

A cover letter is required for consideration for this position and should be attached as the first page of your resume. The cover letter should address your specific interest in the position and outline skills and experience that directly relate to this position.

Seeking a highly motivated, responsible, and detail-oriented Clinical Research Technician to work collaboratively with project managers, program staff, therapists and investigators on a clinical trial examining effective treatments for PTSD.

Experience as part of a team with all 8 competency domains is expected:

1. Scientific Concepts and Research Design
2. Ethical Participant Safety Considerations
3. Investigational Products Development and Regulation
4. Clinical Study Operations (GCP's)
5. Study and Site Management
6. Data Management and Informatics
7. Leadership and Professionalism
8. Communication and Teamwork

Position Specific Responsibilities will Include:

Recruits patients to studies:

• Initiates identification, determines eligibility, and conducts recruitment and retention of study subjects per study protocol.

Data collection activities including all stages of data collection:

• Schedule and conduct follow-up visits with patients at participating sites, complete CRF,maintain accurate data entry in all study databases.

Miscellaneous Research Support:

• In collaboration with investigators and project coordinators, may prepare sections of working papers, progress reports, final reports, and other research reports for submission.
• Conducts literature searches, abstracts articles, prepares summaries and critiques of literature.

* Associate degree in Health Science or an equivalent combination of related education and experience is necessary.

• Minimum 1 year of directly related experience in clinical research and clinical trials is necessary. (Please review SoCRA's Definition of a Clinical Research Professional For qualifying experince prior to applying.) or
• And advanced degree in a health-related areas such as: Health Sciences; Behavioral Sciences; Public Health, Health Care Administration, Clinical Research Administration, Social Work, Psychology, Epidemiology, Foreign MD or
• Minimum 3 years of human subject experience (clinical, lab or health regulations) such as related patience care, related community health and wellness, related clinical information, and research.

The candidate for this position must be able to:

• Demonstrate a strong ability to establish rapport with individuals at all levels including patients and clinicians
• Demonstrate a strong ability to keep accurate and detailed project records
• Working knowledge of all aspects of research including IRB, recruitment and follow-up, protocol management
• Be flexible and work well independently. Candidate must have access to their own reliable transportation

* Bachelor's degree in Health Science or an equivalent combination of related education and experience is desirable.

• An understanding of medical terminology, experience in a large complex health care setting, ability to effectively communicate with staff and faculty of all levels, and knowledge of university policies and procedures is desirable.
• Experience with high-risk populations/topics: PTSD, mental health, suicide, substance use, under-served vulnerable populations, especially interest/enthusiasm in research improving quality and access to treatment for under-served patient populations is strongly preferred.
• Experience with conducting clinical research is preferred. Understanding of HIPAA rules and regulations.
• Comfort discussing sensitive topics with vulnerable populations is necessary.
• Experience and comfort working in clinical settings is preferred.
• Ability to manage day-to-day activities of assigned research projects for ensuring adherence to study protocols.
• Demonstrate motivation and interest.
• Ability to work independently and seek guidance when appropriate, adjust to varying amounts of workload, use time efficiently, take initiative to problem-solve.
• Knowledge of word processing, spreadsheet, database management, audiovisual presentation, and reference management software such as Microsoft Word, Excel, Access, PowerPoint, Qualtrics, and REDCap.
• Possess excellent communication skills, both written and verbal.
• Exhibit exceptional ability to independently prepare correspondence (especially clear, concise, and polite e-mail messages) and write/edit/produce reports.
• Critical thinking and attentiveness to detail required.
• Bilingual proficiency in Spanish, including speaking, reading, and writing, is preferred but not required.

This is a full time, hybrid position. The schedule is mostly Monday through Friday, 8AM - 5PM however some evenings and weekends may be required.