We are currently looking for a Clinical Research Coordinator to join our Health Care Organization based in North Carolina (Pulmonary, Sleep Medicine, Primary and Urgent Care).
You will be responsible for administering questionnaires and subject material, adhering to regulatory trial standards, and participating in subject recruitment efforts, among other duties.
You will need to engage with research subjects, explain what is expected of them, and understand their concerns, requiring excellent interpersonal and communicative skills.
JOB SUMMARY:
The Research Coordinator under general direction performs duties associated with coordinating, implementing, and balancing multiple research studies. The Research Coordinator is accountable for delivering established goals and utilizes good judgment, knowledge, and skills in the area of expertise while maintaining expected quality standards.
ESSENTIAL JOB FUNCTIONS:
- Assists research personnel in the implementation of research studies to ensure successful completion of study goals.
- Overseeing the trouble-free running of clinical trials.
- Collecting data obtained from research, coding and analyzing it
- Managing budgets set aside for research
- Communicating with participants regarding study objectives
- Administering questionnaires and monitoring participants to ensure they adhere to the study’s rules
- Liaising with laboratories regarding research findings
- Monitoring the study to ensure that it complies with protocols, is ethically conducted, and follows regulatory standards
- Maintaining research records of study activity, including case report forms, drug dispensation records, or other regulatory forms as per FDA guidelines
- Directing the collection, labeling, storage, and transport of all specimens
- Assists in the recruitment and relationship building of study subjects, arranges study visits, and provides instructions to meet the goals of the study.
- Abstracts or collects data from study subjects and enters information into the designated forms/database to comply with study protocols.
- Maintains inventory of supplies or equipment, and prepares study kits and requisitions before study visits to ensure the appropriate items are available when necessary.
- Identifies and reports issues that may affect the accuracy and quality of study design and implementation to meet study aims.
- Reports work time monthly for Time and Effort Reporting as required by internal and federal policies.
- Other duties as assigned.
JOB QUALIFICATIONS:
- Bachelor/Associate of Science degree in health science, biological sciences, life research, medical technology, or clinical research
- Experience in a medical or research field is preferred.
- Working knowledge in medical terminology, anatomy, physiology, pharmacology, and Microsoft Office computer programs.
Job Type: Full-time
Pay: $75,000.00 - $110,000.00 per year
Benefits:
- 401(k)
- Health insurance
- Paid time off
Experience level:
Schedule:
Application Question(s):
- As a part of the job, you may be asked to go to our Sanford office once a week or as & when required. Do you accept?
- When can you start?
- Please list 2-3 dates and time ranges that you could do an interview.
- What is your pay expectation?
Experience:
- Clinical research: 3 years (Required)
Work Location: In person