Study Coordinator, Asheville NC
- Job Title
- Study Coordinator, Asheville NC
- Job ID
- 27508328
- Location
- Asheville, NC 28715
- Other Location
- Description
-
JOB SUMMARY
This individual will play a key role in assisting in the conduct of clinical trial activities, in accordance with all applicable regulations governing the conduct of clinical trials. 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. Elligo is looking for candidates that are able to recognize and synthesize information about the organizational climate and partner with key individuals to accomplish organizational goals.The candidate, working closely with study team members under the direct supervision of a Study Manager, will support other study team members in order to achieve study objectives and corporate goals, including:
•Develop strong working relationships and maintain effective communication with•study team members.
•Develop strong working relationships and become the point of contact for the clinic as well as the sponsor for clinic related activities.
•Perform patient/research participant scheduling.
•Collect patient/research participant history.
•Data entry and Management.
•Coordinate follow--up care and laboratory procedures.
•Support the collection and review of required essential study documents and reports. Order supportive study supplies (e.g., contracts, IXRS, labkits, 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.
•Coordinate protocol related research procedures, study visits, and follow--up care.•Assist with the screening, recruiting and enrollment of research subjects.•Comply with Elligo, Clinic, and Sponsor policies, standard operating procedures (SOPs) and guidelinesJob Description-Study Coordinator
- Facilitate pre--study, site qualification, study initiation, monitoring visits, and study close out activities.
- Collect, process and ship laboratory specimens.
- Schedule subject visits and procedures.
QUALIFICATIONAND EDUCATION REQUIREMENTS- Associates Degree or BS/BA in Life Science or related discipline
- Previous nursing experience in a clinical setting a plus
- 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.
WORKING CONDITIONS
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.Regular local and regionaltravel is required for this position.The 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 discrimination and harassment. All employment decisions at Elligo are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV Status, sexual orientation, gender identity and/or expression, marital, civil union or domestic partnership status, past or present military service, family medical history or genetic information, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. Elligo will not tolerate discrimination or harassment basedon any of these characteristics. In addition, Elligo will provide reasonable accommodations for qualified individuals with disabilities.
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“I am super passionate about what we are doing at Elligo and feel so fortunate to be a part of it! I haven’t been this excited about a job in years!”
“Having been involved in clinical research for over 10 years, I have found the Elligo model to be truly innovative. From top to bottom, the Elligo team is made up of professionals who use their experience and knowledge to positively affect the need to bring healthcare and clinical research together.”
“Elligo is at the forefront of innovation in the clinical research industry. It’s rewarding to work among such highly motivated and distinguished leaders and visionaries. I start work each day feeling valued and end each day excited to be part of Elligo’s influence on changing the clinical research industry.”
“Working at Elligo has been a very unique experience. I love the fact that I’m surrounded by colleagues who help me learn something new every day. I value their experience and genuinely enjoy the work and projects we are involved with. I love coming to work every day!”