LYNN HEALTH SCIENCE INSTITUTE
Career Opportunities at Lynn Institute
Lynn Institute is looking for clinical trial investigators and staff to join our team.
Lynn Institute Careers
OKC Corporate Location
Patient Recruitment Associate
QUALIFICATIONS:
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required
ESSENTIAL DUTIES AND RESPONSIBILITIES:
- Answer incoming calls for all sites from advertising placed in local markets.
- Make outgoing calls from call list provided by research, physician, and vendor databases.
- Obtain and verify patient information through data entry in the Clinical Trial Management System.
- Collect patient information through general and study specific phone screens through the Clinical Trial Management System.
- Enter data directly into the Clinical Trial Management System to create searchable and traceable data.
- Inform patients of clinical trials by explaining procedures; answering questions; providing information and feedback.
- Determines eligibility for clinical trials by comparing patient information to study requirements.
- Respond by phone and email to patient inquiries and patient referrals for clinical trials.
- Schedule patients that qualify for clinical trials through the Clinical Trial Management System.
- Provided additional support for all sites needing follow up calls in trials, support as requested by site directors.
- Performs other duties as assigned.
To apply please send your resume to Tacha at tarledge@lhsi.net. View detailed job description here.
Lynn Institute Careers
Denver Location Clinical Research Coordinator
DESCRIPTION:
Coordinates clinical research program by identifying and assessing patients, distributing information, acting as a clinical resource for the study physician’s, sponsor representatives and patients, conducting follow-up care for patients, attending meetings pertaining to the clinical trials.
ESSENTIAL DUTIES AND RESPONSIBILITIES
- Conducts clinical research studies according to study sponsor requirements in conjunction with FDA and ICH/GCPs guidelines.
- Conduct clinical research studies according to designated pharmaceutical sponsor’s protocol
- Provide documentation of all study procedures conducted in a clinical trial.
- Recruit and maintain patients in assigned studies.
- Perform necessary protocol-related procedures.
- Screen potential patients both via phone and in office.
- Maintain adequate study medication documentation.
- Keep investigators updated on patient’s status and any changes in the patient’s medical condition that the patient has not reported to the doctor.
To apply please send your resume to Tacha at tarledge@lhsi.net.