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Site Manager (CRC)

Company: Accel Research Sites
Location: Athens
Posted on: November 8, 2019

Job Description:

Experience : 2 years Research Experience, Dermatology experience Location: Athens Georgia Classification: Full time, Salary Exempt Key Roles: Visit Conduct, Data Entry, Customer Service, Study Oversight Travel: Minimal, Locally Compensation: 50k, Depending on Experience Calling all Clinical Research Rock Stars Join a company that will foster your growth and offer exceptional career opportunities. We are looking for an experienced licensed RN or NP to join our Integrated Site Network team. Willing to consider very experienced non-nurse candidates as well. This position will work primarily with Derm patients and should have a background reflecting previous experience working in a similar medical environment. Work as an integral member of Accel Research Sites staff maintaining the day-to-day relationship with patients and assist in the development of the ARS network. This includes planning, coordinating and, as appropriate, execution of clinical studies in accordance with the protocol, contracted scope of work, Sponsor, CRO, and ACR SOP's and any relevant local guidelines and regulations. The Clinical Research Coordinator will plan, direct, or coordinated clinical research projects. In addition, they will be expected to direct the activities of workers engaged in clinical research projects to ensure compliance with protocols and overall clinical objectives. This position is full time with full benefits, 401K, seven (7) paid holidays, potential bonus program, (PTO) Paid Time Off, and flexible scheduling. Primary Responsibilities: Ensure that the ISN site is appropriately equipped, establish secure storage areas, and necessary training for staff members Work directly at patient/subject interface at research sites to deliver high-quality patient data in accordance with local regulations, agreed scope of work and as required by protocol Attend and participate in investigator meetings, monitoring visits, audits, seminars, and other regional or national meetings Assist with screening and enrollment of subjects into assigned studies Support subjects on trials to encourage maximum retention and future recruitment Assist with the establishment of a recruitment and contingency plan for each study Perform functions necessary for successful completion of all protocol required visits/procedures such as vital signs, phlebotomy, diagnostic tests, dispensing of investigational product, scheduling, drug accountability/reconciliation, and organizational tasks, where appropriate and as delegated by the investigator, in accordance with state/federal requirements Accurately complete source documents and case report forms in both paper and electronic format Assist investigator with recording and reporting of adverse events and SAE's as per local regulatory authority guidelines Communicate effectively across all departments company-wide providing information by telephone, in written form, e-mail, or in-person Required Knowledge, Skills, and Abilities: Sound knowledge of medical terminology Sound knowledge of ICH/GCP and regulatory requirements Excellent interpersonal and organizational skills Proficient in the use of Microsoft Office and Excel Fluent in English, spoken and written Ability to work independently, actively prioritize among multiple competing tasks, seek input, and problem solve Ability to maintain confidentiality Ability to establish and maintain effective working relationships with coworkers, managers and clients Minimum Required Education, Experience, and Certifications: Maintain License/Certification status of CCRC IATA Certification Skilled in Phlebotomy Good Clinical Practice (GCP) Clinical Research Coordinator experience Experience in Dermatology Position Type/Physical Demands: This is a full-time position. Days and hours of work are typically Monday through Friday, 7:00 a.m. to 4:00 p.m., hours may change/vary per business needs. Walking, standing, some bending, stooping and stretching. Requires hand-eye coordination and manual dexterity sufficient to operate a keyboard, photocopier, telephone, calculator and other office equipment. Requires normal range of hearing and eyesight to record, prepare and communicate appropriate reports. Requires occasional lifting of boxes up to 50 pounds. Work is performed in a medical office environment and includes exposure to blood-borne pathogens and bio-hazardous materials. This role requires the ability to work with a broad range of personalities, situations and psychiatric disorders; therefore, candidates must possess the ability to resolve conflicts immediately and diffuse potentially escalating events before they occur. Disclaimer: Please note that while this job description is intended to be an accurate reflection of the current role, it is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Management reserves the right to revise duties, responsibilities, skills, efforts, or adjust the scope of the job at any time, as necessitated by business demands.

Keywords: Accel Research Sites, Athens , Site Manager (CRC), Executive , Athens, Georgia

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