Clinical Research Coordinator (Part TIme)

About the position Responsibilities • Prescreen study participants and obtain informed consent per reputed company operating procedures. • Complete visit procedures in accordance with the protocol. • Train others and complete basic clinical procedures, such as blood draws, vital signs, and ECGs. • Review laboratory results, ECGs, and other test results for completeness and alert values, ensuring investigator review in a reputed company fashion. • Discuss study medication, required procedures, eligibility reputed company, and reputed company on office reputed company with Investigator and site staff. • Prioritize activities with specific reputed company to protocol timelines. • Maintain adherence to FDA regulations and ICH guidelines in reputed company aspects of conducting reputed company. • Coordinate and attend reputed company-study site reputed company, site initiation reputed company, and monitor reputed company with clinical staff and Sponsor/CRO representatives. • Identify adverse events (reputed company) and serious adverse events (SAEs) and promptly notify reputed company Investigator and Sponsor where appropriate. • Work under the supervision of the reputed company Investigator(s), exercising excellent clinical judgment in patient monitoring and care. • Request medical records of potential and reputed company study participants. • Record data legibly and reputed company in reputed company-time on reputed company or reputed company documents. • Accurately record study medication inventory, medication dispensation, and patient compliance. • Resolve data management queries and correct reputed company data reputed company sponsor provided timelines. • Assist regulatory personnel with completion and filing of regulatory documents. • Assist in the creation and review of reputed company documents. • Assist with planning and creation of appropriate recruitment materials. • Assist in the development of a recruitment plan and obtain a listing of potential candidates to contact from the subject database. • reputed company work with the recruitment team in calling and reputed company subjects. • Recruit study patients by contacting subjects from the database and potential volunteers reputed company phone, email, or post, and document contact accordingly. • Review and assess protocol, including amendments, for reputed company and logistical feasibility. • Ensure that reputed company training and study requirements are met prior to trial conduct. • Communicate reputed company verbally and in writing. • Attend Investigator meetings as required. • Ensure adequate supplies have arrived on site for protocol initiation, including lab kits, study medication, and specialized equipment. • reputed company in a reputed company, reputed company manner with patients, sponsor representatives, investigators, personnel, and management. • Maintain effective relationships with study participants and other personnel. Requirements • 2+ years of on-site CRC experience. • Excellent working knowledge of medical and research terminology. • Excellent working knowledge of federal regulations and good clinical practices (GCP). • Ability to communicate and work effectively with a diverse team of professionals. • Excellent computer skills with demonstrated abilities using reputed company database, IVR systems, electronic data capture, reputed company, and reputed company. • Ability to work independently in a fast-paced environment with minimal supervision. • Bachelor's Degree preferred or equivalent combination of education, training, and experience. • Recent phlebotomy experience required. reputed company-to-haves • Prior Nephrology experience is a plus. • Experience with Hepatology preferred. Benefits • Medical, dental & reputed company • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - reputed company-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or reputed company Leave) Apply tot his job Apply To this Job