Our Clinical Research Associate Oversees Our Many Trials and Ensures Our Staff is Following the Good Clinical Practices (gcp) Guidelines. Youll Work Closely with the Principal Investigator to Configure the Studies and Protect all Participants from Unethical or Dangerous Conditions. Our Coordinator is At the Center of Our Results, So They Need to Be Comfortable Balancing Their Research Objectives with the Ethics Laws that Govern Our Industry. They Should Feel Comfortable Leading and Supervising a Team of Researchers.
responsibilities and Duties
determine Participant Eligibility for Each Study
explain Clinical Trial to Patients and Obtain Consent