Clinical Research Study Coordinator Poway, CA
Company: Elligo Health Research
Location: Poway
Posted on: August 2, 2022
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Job Description:
Job 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. The employee, 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. 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,
nonclinical 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. QUALIFICATION AND EDUCATION REQUIREMENTS Associates
Degree or BS/BA in Life Science or related discipline Previous
nursing experience in a clinical setting a plus At least one year
of experience in coordinating clinical trials Prior training in GCP
requirements 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 regional travel 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 based on any of these
characteristics. In addition, Elligo will provide reasonable
accommodations for qualified individuals with disabilities.
Keywords: Elligo Health Research, Poway , Clinical Research Study Coordinator Poway, CA, Healthcare , Poway, California
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