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 Clinical Research Coordinator - San Antonio

Details
Country: USA
Location: TX San Antonio
Total applied: 8

Relevant Work Experience: 2+ to 5 Years
Career Level: Experienced (Non-Manager)
Education Level: High School or equivalent
Job Type: Employee
Job Status: Full Time

Clinical Research Coordinator - San Antonio

Clinical Research Coordinator - San Antonio

Radiant Research, a company of leading clinical research sites, has experienced rapid growth at our San Antonio - Medical Center location. Radiant Research exclusively focuses on providing professional, high quality clinical research services to the pharmaceutical industry while also providing a critical service to study participants by making investigational therapies available in a controlled environment.

 

We are seeking a full time Clinical Research Coordinator for our San Antonio Texas site. Working under the supervision of the Principal Investigator and Site Director, this position will coordinate the conduct of clinical drug studies from pre-study planning through successful completion of all patient visits and documentation. The Coordinator is directly involved in patient care.

Job Responsibilities include:

1.  Maintain a high level of knowledge and understanding of assigned protocols, including all protocol requirements for patient visits, obtaining informed consent, patient visit schedules, test, procedures, laboratory information, and drug accountability requirements.

2.  Responsible for completion of all study documentation forms, including case report forms and other study specific documents.

3.  Coordinate and conduct patient care visits and assure all procedures are conducted in compliance with the clinical protocol.

4.  Interact with Principal Investigator as needed to assure patient receives appropriate medical evaluation and care when needed, alerts Principal Investigator of serious adverse events.

5.  Interacts with sponsor Clinical Research Associate to facilitate the sponsor monitoring and database clean-up process.

6.  Attends sponsor Investigator/Study Coordinator meetings as needed for assigned protocols

7.  Conducts clinical research in compliance with all applicable regulations.

 

 REQUIREMENTS

Qualifications:

1.  At least two years of recent experience in a clinical setting

2.  Prior clinical research experience strongly preferred

3.  Ability to work well with co-workers, peers, monitors and potential subjects.

4.  R.N. or L.V. N. currently licensed in TX preferred

5.  Ability to effectively and efficiently handle multiple tasks simultaneously with precision and adhere to sponsor requirements

6.  The candidate should be able to promote a teamwork philosophy with a positive attitude.

We provide a dynamic environment, a competitive benefits package with medical, dental, and vision coverage, life and disability insurance, and 401K, and the opportunity to grow with us.

 

To Apply:

Please respond via e-mail to martharicketson@radiantresearch.com .

 

Radiant Research is an Equal Opportunity Employer.

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