Job Focus
- Inform patients or caregivers about study aspects and outcomes to be expected.
- Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.
- Maintain required records of study activity including case report forms, drug dispensation records, or regulatory forms.
- Communicate with laboratories or investigators regarding laboratory findings.
- Order drugs or devices necessary for study completion.
- Complete the requisition, collection, labeling, storage, or shipment of specimens.
- Arrange for research study sites and determine staff or equipment availability.
- Perform specific protocol procedures such as interviewing subjects, taking vital signs, and performing electrocardiograms.
- Develop advertising and other informational materials to be used in subject recruitment.
- Determine best recruitment practices for studies and implement.
- Organize study equipment and supplies.
- Track enrollment status of subjects and document dropout information such as dropout causes and subject contact efforts.
- Record adverse event and side effect data and confer with investigators regarding the reporting of events to sponsor and IRB.
- Obtain informed consent and document process.
- Dispense drugs and provide instructions as necessary.
- Contact outside health care providers and communicate with subjects to obtain follow-up information.
- Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, and discussions with physicians and nurses.
- Schedule subjects for appointments, procedures, or inpatient stays as required by study protocols.
Your Profile
- Team Player
- Strong Oral Communication Skills
- Excellent customer service and interpersonal skills
- Fast, Efficient, Organized, Highly Motivated, Professional, Punctual, and Ability to Multi-Task
- Experience with Research & Clinical Trials Protocols & Procedures
- Dermatology Knowledge is a plus
- Proficient with Computers
- Authorized to work in the US
Qualifications
- Research & Clinical Trials Experience (at least 2 years)
- Phlebotomy Certified (Preferred)
Job Type: Full-time
Job Type: Full-time
Pay: From $50,000.00 per year
Benefits:
Schedule:
Education:
Experience:
- Clinical Trials: 2 years (Preferred)
- Clinical Research: 2 years (Preferred)
Language:
Work Location: In person