Clinical Research Sub-Investigator, Nurse Practitioner

Cliantha Research – North America, is currently seeking a Sub Investigator, Nurse Practitioner for our St. Pete site, who can fulfill its business needs and provide world class leadership to the team.

About Us

Cliantha Research is a full-service Clinical Research Organization (CRO) that provides comprehensive and integrated offerings in Early Phase, Late Phase, Respiratory, Dermatology, Consumer Research, Research Lab, IVRT, Biometrics, Pharmacovigilance & Medical Services, and Environmental Exposure Chambers (EECs).Cliantha Research is headquartered in Ahmedabad and has expanded its domestic presence with 5 regional offices & international presence with offices in USA (Florida), Canada (Mississauga, Winnipeg & Scarborough) & Europe (Portugal).

Overview of Role

We are looking for a seasoned Nurse Practitioner to become our Sub Investigator and direct and oversee all research activities and foster a culture of research integrity within our St. Petersburg FL location. As sub-investigator, they will be responsible for assisting in the overall conduct of the clinical trials conducted here under direction of the Principal investigator. Provide direct back-up as an Investigator, under the direction of the Principal Investigator and within the functions allowed for anARNP for Cliantha Research.

Key Expectations for the Role

• Provide clinical and medical support and oversight for research clinical trials based on scope of practice; obtain complete study participant history, conduct physical exams, review medical charts, assess findings, prescribe and re-fill medication, and perform designated procedures according to written protocols.
• Assess, grade, and document adverse events; apply triage and judgment to determine course of action.
• Reviews and interprets clinical laboratory tests, ECGs, medical history data, and other clinical information regarding potential and enrolled study subjects to evaluate eligibility or ongoing participation
• Acts as part of a multidisciplinary team to provide continuity of care to patients throughout various stages of treatment on protocol and follow-up.
• Comply with institutional policies, standard operating procedures, and guidelines; prepare and submit documentation as required by the study protocol and study sponsor; interpret complex protocols. Coordinate and collaborate with Principal Investigator to review study protocol.
• Review and approve final study reports or other clinical documents.
• Ensure optimal study conduct.

What you’ll bring:

To perform this job successfully, an individual must have:

• Licensed Nurse Practitioner
• A minimum of 1 or more years of experience in a clinical research position
• Requires a thorough knowledge of the: Drug development process, Clinical trial management, Clinical monitoring, FDA regulations, ICH Good Clinical Practice, and Good Documentation Practice, HIPAA
• Phlebotomy skills
• Strong analytical and problem-solving skills
• Excellent organizational skills, detail oriented, efficient, and able to multi-task and prioritize effectively.
• Excellent interpersonal skills.
• Strong written and verbal communication skills
• Bilingual skills preferred.

Full-Time On-site Position

This role is a full-time role within Cliantha and qualifies for up to 80 hours of PTO as well a vacation time annually, in addition to a generous health and benefits package.

Why Cliantha?

Cliantha is on the cutting edge of clinical trials. If you are interested in being part of the next breakthrough in clinical trial research, then we are looking for you!

Job Type: Full-time

Pay: From $107,000.00 per year

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Paid time off
• Vision insurance

Schedule:

• 10 hour shift
• 12 hour shift
• 8 hour shift
• Day shift
• Evening shift
• Monday to Friday
• Night shift
• Overtime
• Weekends as needed

People with a criminal record are encouraged to apply

Ability to commute/relocate:

• Saint Petersburg, FL 33714: Reliably commute or planning to relocate before starting work (Required)

Experience:

• Clinical Trials: 1 year (Required)

License/Certification:

• Certified Nurse Practitioner (Required)

Work Location: In person