RN Pharmacy Research Coordinator
Listed on 2026-01-01
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Healthcare
Clinical Research -
Research/Development
Clinical Research
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Job Summary
The RN / Pharmacy Coordinator assists in the conduct of clinical trial activities, in accordance with all applicable regulations governing the conduct of clinical trials. This position will be responsible for working onsite full time at the Elligo CRC as an Unblinded Pharmacist for applicable CRC studies, performing Drug Reconstitution, Injections, and serve in an unblinded role for Investigational Product prep and administration.
Job Summary
The RN / Pharmacy Coordinator assists in the conduct of clinical trial activities, in accordance with all applicable regulations governing the conduct of clinical trials. This position will be responsible for working onsite full time at the Elligo CRC as an Unblinded Pharmacist for applicable CRC studies, performing Drug Reconstitution, Injections, and serve in an unblinded role for Investigational Product prep and administration.
The primary skills include logical thinking, ability to prioritize, “can-do” attitude, the ability to adapt quickly to changing business conditions, strong interpersonal and team building skills.
RESPONSIBILITES
- Will take primary role as for study related pharmacy tasks and serve in unblinded pharmacist role for applicable trials.
- Develop strong working relationships and maintain effective communication with
- Become the point of contact for the clinic as well as the sponsor for clinic related activities.
- Manage multiple concurrent trials
- Completes all protocol related training
- Perform patient/research participant scheduling
- Collect patient/research participant history
- Collects and maintains source documentation
- Performs data entry and query resolution
- Support the collection and review of required essential study documents and reports. Order supportive study supplies (e.g., contracts, IXRS, lab kits, non- clinical supply materials, imaging and laboratory handling manuals, etc.).
- Adhere to an IRB approved protocol
- Assist in the informed consent process of research subjects.
- Support the safety of research subjects, report adverse events.
- Coordinate protocol related research procedures, study visits, and follow-up
- Assist with the screening, recruiting and enrollment of research subjects.
- Facilitate pre-study, site qualification, study initiation, monitoring visits, and study close out activities
- Collect, process and ship laboratory specimens
- Comply with Elligo, Clinic, and Sponsor policies, standard operating procedures (SOPs) and guidelines.
Skills And Abilities
Required
- RN, MSN, PTCB with CPhT, or a related field and a minimum of 5 years of experience in a healthcare setting, or an equivalent combination of education and experience.
- Associates Degree or BS/BA in Life Science or related discipline
- Strong interpersonal skills with attention to detail a must.
- Demonstrated proficiency with word processing, spreadsheet, database, and presentation software (MS Office skills such as Outlook, Word, Excel, PowerPoint, SharePoint) and with clinical trial master filing systems.
This job operates in a professional office environment. This role routinely uses standard office equipment such as computers, phones, and photocopiers.
Some flexibility in hours is allowed, but the employee must be available during the “core” work hours of 9:30 a.m. to 3:30 p.m. and must work 37.5 hours each week to maintain full-time status. Occasional evening and weekend work may be required as job duties demand.
Travel:
Local and Regional
he above statements are intended to describe the general nature and level of work being performed by individuals assigned to this position. They are not intended to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel. More in-depth information can be found in SOP's, working guidelines, policies, etc.
Elligo is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of…
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