Clinical Trials and Medical Research Studies in Columbus Ohio

Medical Miracles come from Everyday Heroes.

Clinical Research Office in Columbus seeking a part time.

Regulatory Coordinator

Responsibilities for this position will be to coordinate, review, maintain and prepare documentation packages for pharmaceutical regulatory submission to IRB’s. These submissions include initial application, 1572’s, INDs/INDSR’s, and annual reports.

Ideal candidates must have 2+ years of Regulatory experience, strong organizational and computer skills. Candidates must be pleasant, responsible and maintain confidentiality.

Interested candidates send resume along with salary requirement to amclellan@columbusclinical.com

Clinical Research Office in Columbus seeking full time.

Clinical Research Coordinator

Responsibilities : To perform clinical procedures that include drawing blood, taking vital signs, administering medications, conducting monitoring visits with pharmaceutical representatives, updating and reviewing regulatory documents, and being able to identify and recruit potential patients.

Requirements: At least 2 years experience in clinical research. Must demonstrate a strong attention to detail and organization. Computer skills and good communication are a must. A strong knowledge of commitment and adherence to FDA and IRB regulations. Must be able to work as a team member and adhere to flexibility.

Education Requirements: College degree a must. Preferred in BS, LPN or RN.1-2 years related experience in the health care field.

Interested candidates please email resumes to amclellan@columbusclinical.com