Sub-Investigator

Civia Health; Lewes; On-site; GBP 45,000 - 60,000; Full time

Job summary

An innovative clinical research company in Lewes is looking for a Nurse Practitioner to conduct study visits and ensure quality compliance in clinical trials focused on metabolic conditions. Ideal candidates should have an active Nurse Practitioner license and relevant clinical research experience. The role offers competitive compensation along with medical insurance and professional development support.

Benefits

Competitive compensation

Medical, dental, and vision insurance

Generous PTO and paid holidays

Flexible scheduling options

Professional development support

Qualifications

• 2+ years of clinical research experience, preferably in Phase 2–4 trials.
• Experience with GLP‑1 therapies or metabolic/endocrine research highly preferred.
• Strong knowledge of GCP/ICH guidelines; certification is a plus.

Responsibilities

• Conduct study visits, including medical assessments and physical exams.
• Partner with principal investigators to ensure quality and regulatory compliance.
• Engage participants, providing clear education and ensuring comfort.

Skills

Clinical research experience

Communication skills

Attention to detail

Collaborative spirit

Education

Active Nurse Practitioner license

Job description

Overview

Job Type: on-site. Reports to: Medical Director. Join Civia Health, an innovative clinical research company focused on metabolic conditions and GLP‑1 therapies. We aim to bring clinical trials to the community, making them accessible, inclusive, and participant‑centered.

Responsibilities

• Conduct study visits, including medical assessments, physical exams, and protocol‑specific procedures.
• Partner with principal investigators and research staff to ensure quality, safety, and regulatory compliance.
• Engage participants with empathy—providing clear education, answering questions, and ensuring comfort throughout the trial process.
• Identify, document, and report adverse events per protocol and regulatory standards.
• Maintain accurate, timely, and high‑quality documentation in source records and EDC systems.
• Contribute to continuous improvement of workflows and study execution with a team‑first mindset.
• Occasional travel may be required for audits, site visits, or team meetings.

Qualifications

• Active, unrestricted Nurse Practitioner license.
• 2+ years of clinical research experience (Phase 2–4 trials preferred).
• Experience with GLP‑1 therapies or metabolic/endocrine research highly preferred.
• Strong knowledge of GCP/ICH guidelines; certification is a plus.
• Excellent clinical judgment, attention to detail, and communication skills.
• A collaborative spirit and commitment to doing what’s best for the patient and the team.

Benefits

• Competitive compensation.
• Medical, dental, and vision insurance.
• Generous PTO and paid holidays.
• Flexible scheduling options.
• Professional development and continuing education support.
• Mission‑driven team that values respect, inclusion, and innovation.

Ready to make an impact? Apply by submitting your resume and cover letter to the link above. We’re excited to learn more about you!