Chear Center LLC - International Medical Graduate/ Research Coordinator

May 10, 2019

 

Part-time

This individual will be responsible for conducting and managing subject research visits at clinic by following protocols and Standard Operating Procedures (SOPs). Responsibilities include:

  • Conduct multiple clinical trial research subject visits by closely following the trial specific protocol in accordance with GCP and FDA guidelines.

  • Coordinate the day-to-day research activities at the clinic under the supervision of Principal Investigator (Licensed MD).

  • Review, extract and analyze data from medical charts for initial screening/identification of eligible subjects.

  • Assess protocol inclusion/exclusion criteria and confirms eligibility of subjects.

  • Recruits and interviews prospective subjects for clinical studies. Familiarizes potential subjects with the details of the study through phone contacts and personal interviews.

  • Ensures that the informed consent process has occurred, is properly documented and filed as required.

  • Recognizes AEs (adverse events) and SAEs (serious adverse events) and promptly notifies appropriate parties; e.g. Principal Investigator, Study Sponsor, and IRB.

May complete basic clinical procedures such as phlebotomy , ECGs, pulmonary function tests and obtaining blood pressure.

Job Types: Full-time, Part-time

Experience:

  • IMG/FMG (license not required): 1 year (Preferred)

Education:

  • Doctorate (Required)

Language:

  • spanish (Preferred)

     

     

     

     

     

     

     

     

     

Apply on Indeed: 

https://www.indeed.com/viewjob?jk=07d76c0e48189945&from=myjobs&tk=1dac5te6d0nf7000

 

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