Evolution Research Group
Clinical Research Pharmacy RN-PRN
Evolution Research Group, Fort Myers, Florida, United States, 33916
Clinical Research Pharmacy RN‑PRN
Join to apply for the Clinical Research Pharmacy RN‑PRN role at Evolution Research Group. About Us
Evolution Research Group (ERG) is dedicated to delivering high‑quality Phase I–IV clinical trial execution to help sponsors bring lifesaving and life‑enhancing therapies to market quickly and safely. Founded in 2014, ERG has grown into a leading neuroscience clinical development company with affiliate sites across the U.S. and deep expertise in clinical pharmacology, psychiatry, neurology, acute pain, and metabolic disorders. ERG has completed over 5,000 trials and continues to expand into high‑need therapeutic areas in the U.S. and globally. Why join us?
We offer a supportive culture, meaningful work, and the opportunity to contribute to cutting‑edge research alongside industry leaders. Competitive benefits include medical and dental coverage, a matching 401(k), and paid time off. Job Description
The RN will prepare and dispense investigational drugs and materials issued by the company for ongoing research studies. In executing these responsibilities, the Research RN is guided by Good Clinical Practices (GCP), International Committee on Harmonization (ICH) guidelines, and company standard operating procedures. This role is approximately 25 hours per week, with flexibility for additional hours and days. Pharmacy Activities
Develop step‑by‑step procedures and/or kits for preparation, dispensing, and distribution of investigational and study drug. Develop codes, labels, and other predefined formats for pharmacy computer entry. Establish and maintain adequate and easily retrievable record‑keeping systems for protocols, study subjects, drug inventory, and dispensing of investigational drugs per regulatory and ICH requirements. Develop staff training regarding investigational and study drug procedures; train Research Pharmacy Technicians, clinical research coordinators, or delegated staff in preparation, labeling, record‑keeping, dispensing, and kit utilization. Prepare drug data sheets and other documents for Research Pharmacy Technicians. Establish and maintain standards that assure quality, proper storage, and safe use of all investigational agents and related supplies. Delegate ordering and stocking of investigational and study agents to the Research Pharmacy Technicians, ensuring protocol compliance. Delegate removal and disposal of expired stock or stock from completed or terminated studies, ensuring protocol compliance. Ensure paperwork is completed and retained, and that investigational and study drugs are handled according to sponsor requirements. Prepare special formulations of investigational agents under unusual circumstances as dictated by a particular protocol. Assist with the development of statistical reports and activity summaries as appropriate monthly; reports will be submitted to the Medical Director, Site Director, and Senior Clinical Research Coordinator for review. Assist with monthly pharmacy audits to ensure company policies and procedures are met; assist in quality assurance procedures as needed. Maintain a neat and clean work area; develop a well‑organized work routine. Additional responsibilities may be assigned as required by the evolving needs of the organization. Skills & Qualifications
Education and Experience
Graduate/completion of an approved accredited school of nursing. Valid RN license in the state of practice; current license maintenance required. Minimum of one (1) year of clinical research experience. CPR certification required; ACLS preferred for RN. Phlebotomy certification (national) preferred. Understanding of regulatory requirements, GCP, and ICH guidelines. Strong communication and collaboration skills with providers, co‑workers, and others. Knowledge of medical terminology for communication with physician offices and staff. Ability to initiate or modify behavior to achieve desired outcomes despite environmental factors.
Requirements
Ability to work independently and as a team player. Ability to organize and prioritize within a changing environment. Use of safety/universal precautions to protect self, subjects, and staff. Appropriate implementation of protocol and regulatory requirements in study conduct. Proficient in venipuncture, centrifugation, sample storage, and performing electrocardiogram. Excellent documentation practices. Good organizational and interpersonal skills. Attentive to detail, good initiative, and ability to work with changing priorities.
Seniority level: Entry level. Employment type: Full‑time. Job function: Health Care Provider. Industries: Research Services.
#J-18808-Ljbffr
Join to apply for the Clinical Research Pharmacy RN‑PRN role at Evolution Research Group. About Us
Evolution Research Group (ERG) is dedicated to delivering high‑quality Phase I–IV clinical trial execution to help sponsors bring lifesaving and life‑enhancing therapies to market quickly and safely. Founded in 2014, ERG has grown into a leading neuroscience clinical development company with affiliate sites across the U.S. and deep expertise in clinical pharmacology, psychiatry, neurology, acute pain, and metabolic disorders. ERG has completed over 5,000 trials and continues to expand into high‑need therapeutic areas in the U.S. and globally. Why join us?
We offer a supportive culture, meaningful work, and the opportunity to contribute to cutting‑edge research alongside industry leaders. Competitive benefits include medical and dental coverage, a matching 401(k), and paid time off. Job Description
The RN will prepare and dispense investigational drugs and materials issued by the company for ongoing research studies. In executing these responsibilities, the Research RN is guided by Good Clinical Practices (GCP), International Committee on Harmonization (ICH) guidelines, and company standard operating procedures. This role is approximately 25 hours per week, with flexibility for additional hours and days. Pharmacy Activities
Develop step‑by‑step procedures and/or kits for preparation, dispensing, and distribution of investigational and study drug. Develop codes, labels, and other predefined formats for pharmacy computer entry. Establish and maintain adequate and easily retrievable record‑keeping systems for protocols, study subjects, drug inventory, and dispensing of investigational drugs per regulatory and ICH requirements. Develop staff training regarding investigational and study drug procedures; train Research Pharmacy Technicians, clinical research coordinators, or delegated staff in preparation, labeling, record‑keeping, dispensing, and kit utilization. Prepare drug data sheets and other documents for Research Pharmacy Technicians. Establish and maintain standards that assure quality, proper storage, and safe use of all investigational agents and related supplies. Delegate ordering and stocking of investigational and study agents to the Research Pharmacy Technicians, ensuring protocol compliance. Delegate removal and disposal of expired stock or stock from completed or terminated studies, ensuring protocol compliance. Ensure paperwork is completed and retained, and that investigational and study drugs are handled according to sponsor requirements. Prepare special formulations of investigational agents under unusual circumstances as dictated by a particular protocol. Assist with the development of statistical reports and activity summaries as appropriate monthly; reports will be submitted to the Medical Director, Site Director, and Senior Clinical Research Coordinator for review. Assist with monthly pharmacy audits to ensure company policies and procedures are met; assist in quality assurance procedures as needed. Maintain a neat and clean work area; develop a well‑organized work routine. Additional responsibilities may be assigned as required by the evolving needs of the organization. Skills & Qualifications
Education and Experience
Graduate/completion of an approved accredited school of nursing. Valid RN license in the state of practice; current license maintenance required. Minimum of one (1) year of clinical research experience. CPR certification required; ACLS preferred for RN. Phlebotomy certification (national) preferred. Understanding of regulatory requirements, GCP, and ICH guidelines. Strong communication and collaboration skills with providers, co‑workers, and others. Knowledge of medical terminology for communication with physician offices and staff. Ability to initiate or modify behavior to achieve desired outcomes despite environmental factors.
Requirements
Ability to work independently and as a team player. Ability to organize and prioritize within a changing environment. Use of safety/universal precautions to protect self, subjects, and staff. Appropriate implementation of protocol and regulatory requirements in study conduct. Proficient in venipuncture, centrifugation, sample storage, and performing electrocardiogram. Excellent documentation practices. Good organizational and interpersonal skills. Attentive to detail, good initiative, and ability to work with changing priorities.
Seniority level: Entry level. Employment type: Full‑time. Job function: Health Care Provider. Industries: Research Services.
#J-18808-Ljbffr