Specialist Office Services Limited Hiring for Clinical Research Coordinator at Rockville, MD Full Time

Clinical Research Coordinator

Rockville, MD

MUST:

1 plus years of experience in the clinical research field

Experience with data collection

Experience with patient enrollment and screening

Experience evaluating data

Experience working with investigators

Experience preparing for audits and FDA inspections

Ability to coordinate all phases of clinical research trials

Experience entering and updating information in Clinical Trial

Working knowledge of GCP

Experience preparing budgets for studies

DUTIES:

Clinical Research Coordinator will be responsible for, but not limited to the following:

Oversee, prepare, submit and maintain regulatory submissions

Handle the coordination of clinical research activities of all phases and all levels as well as investigator-initiated research

Attend investigator meetings

Enter data into clinical trial system

Monitor and adverse events

Oversee the informed consent process and review consent forms with research participant

• Quadrant, Inc. is an equal opportunity and affirmative action employer. Quadrant is committed to administering all employment and personnel actions on the basis of merit and free of discrimination based on race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or status as an individual with a disability. Consistent with this commitment, we are dedicated to the employment and advancement of qualified minorities, women, individuals with disabilities, protected veterans, persons of all ethnic backgrounds and religions according to their abilities.