NP/Sub I

Green Life Science; Kentucky; On-site; USD 95,000 - 135,000; Full time

Job summary

Green Life Science is seeking an experienced Nurse Practitioner to join our clinical research team as a Sub-Investigator, supporting Phase I–IV trials. This investigator-level role works closely with the Principal Investigator to ensure safe and compliant conduct of studies.

The ideal candidate has current NP licensure and clinical research experience, with preference for Sub-Investigator background and familiarity with industry-sponsored trials and GCP/ICH/FDA regulations.

Qualifications

• Current NP licensure.
• Clinical research experience.
• Previous Sub-Investigator experience preferred.
• Experience with industry-sponsored clinical trials.
• Knowledge of GCP/ICH/FDA regulations.

Responsibilities

• Conduct medical visits, examinations and clinical assessments of study participants.
• Review medical histories and protocol eligibility criteria.
• Assess treatment response and adverse events.
• Support informed consent and patient safety.
• Review and follow clinical trial protocols.
• Work closely with the PI, research team, sponsors and clinical monitors.
• Participate in investigator meetings, monitoring visits and audits.
• Ensure compliance with GCP, ICH and FDA requirements.
• Support accurate clinical documentation and data integrity.
• Provide input into recruitment, study feasibility and trial execution.

Skills

Clinical research

GCP/ICH knowledge

Independent work

Communication skills

Clinical judgement

Education

Nurse Practitioner license

Job description

We are seeking an experienced Nurse Practitioner to join our clients clinical research team as a Sub-Investigator, supporting Phase I-IV clinical trials.

This is an investigator-level role, working closely with the Principal Investigator and research team to ensure the safe and compliant conduct of clinical trials.

Key Responsibilities

• Conduct medical visits, examinations and clinical assessments of study participants
• Review medical histories and protocol eligibility criteria
• Assess treatment response and adverse events
• Support informed consent and patient safety
• Review and follow clinical trial protocols
• Work closely with the PI, research team, sponsors and clinical monitors
• Participate in investigator meetings, monitoring visits and audits
• Ensure compliance with GCP, ICH and FDA requirements
• Support accurate clinical documentation and data integrity
• Provide input into recruitment, study feasibility and trial execution

Ideal Candidate

• Current NP licensure
• Clinical research experience
• Previous Sub-Investigator experience preferred
• Experience with industry-sponsored clinical trials highly desirable
• Knowledge of GCP/ICH/FDA regulations
• Strong clinical judgement and communication skills
• Able to work independently and collaboratively

Therapeutic Areas

Our client conducts a broad range of clinical research, with particular expertise in neuroscience, neurology, psychiatry, clinical pharmacology, pain and metabolic disorders, alongside other Phase I-IV programmes.

Ideal for an NP who wants to combine their clinical expertise with meaningful involvement in clinical research and take on greater responsibility as a Sub-Investigator.