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Clinical Research Coordinator - CRC - Philadelphia job
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Country: USA
Location: Delaware-Delaware Philadelphia, PA 19019
Total applied: 40 Job Category:Medical/Health
Relevant Work Experience:2+ to 5 Years
Education Level:Associate Degree
Location:Philadelphia, PA 19019
Status:Full Time, Temporary/Contract/Project, Employee
Occupations:Nursing
Career Level:Experienced (Non-Manager)
Relevant Work Experience:2+ to 5 Years
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Clinical Research Coordinator - CRC - Philadelphia job
Become part of an organization that is the cutting edge of research! Group is conducting trials involving OB/GYN and is seeking an experienced CRC to coordinate this research. These are temp-hire opportunities offering top pay for the right candidate. OB/BYN and IV therapy experience strongly preferred.
SUMMARY: Conduct clinical research coordinator duties with principal investigators and sub-investigators in given area. Travel to sites and sub-sites and coordinate protocols. Schedule patients. Interact with patients and investigators as well as site monitors via phone. Complete CRFs as required. Use EDC to complete on-line protocols. Follow SOPs.limited to:
a. Recruit and interview candidates for study eligibility and enrollment
b. manage informed consent process and ensure confidentiality practices are consistent with regulatory and study guidelines
c. maintain a strong relationship with subjects involved in clinical trials and ensure that their rights as subjects are protected
d. coordinate appointments of drug study subjects
e. perform vital signs and EKG’s when necessary
f. dispense and account for drugs used in study
g. log and inform Principle Investigator (PI) of any possible adverse reactions to study medications
h. maintain study log and IRB forms
i. coordinate and maintain professional relationships with Clinical Research Organization’s associate (CRA) and coordinate monitoring visits
j. maintain a strong relationship with investigators and their staff members and entities representing the interests of professionals participating in trials, i.e., Independent Physician Associations
QUALIFICATIONS: 2-3 years minimum experience as Clinical Research Coordinator. Able to travel in a given area. Prefer OB/GYN experience and prefer IV therapy experience / training. Must be compute savvy with EDC experience a plus.
Employees must adhere to drug-free work place policy that requires initial and random drug testing.
reply to : jason.russell@soliant.com
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