A Clinical Investigator works on a clinical trial, and is responsible for ensuring that an investigation is conducted according to the signed investigator statement, the investigational plan, and applicable regulations; for protecting the rights, safety, and welfare of subjects under the investigator's care; and for the control of drugs under investigation. The Clinical Investigator must also meet requirements set forth by the FDA, EMA or other regulatory body. The qualifications must be outlined in a current resume and readily available for auditors.
Clinical Research Sub-Investigator Eligible Applicants:
Nurse Practitioner (NP), Physician Assistant (PA), Medical Doctor (MD), or Doctor of Osteopathic Medicine (DO)
Company:
Chemidox Clinical Trials Location:
Lancaster, California Job Type:
Full-Time Schedule:
Monday-Friday Onsite Compensation:
Competitive salary based on experience, qualifications, and leadership background. About Chemidox Chemidox Clinical Trials is seeking a motivated Nurse Practitioner (NP), Physician Assistant (PA), Medical Doctor (MD), or Doctor of Osteopathic Medicine (DO) to join our growing team as a Clinical Research Sub-Investigator. Chemidox is a fast-growing, multispecialty clinical research organization conducting Phase II-IV clinical trials across a variety of therapeutic areas, including women's health, OB-GYN, internal medicine, cardiology, dermatology, neurology, pediatrics, vaccines, and metabolic disease. We partner with leading pharmaceutical companies and CROs to bring innovative therapies to our community while maintaining a patient-first approach. We value visibility, ownership, teamwork, professional development, and continuous improvement. We believe strong teams are built through open communication, shared accountability, reliable follow-through, and a clear understanding of responsibilities and progress. Position Summary This position is designed for clinicians who want to expand beyond traditional patient care, contribute to advancing medical research, and develop as clinical leaders within a growing organization. Working under the supervision of the Principal Investigator, you will perform protocol-required clinical assessments, protect participant safety, collaborate with research coordinators, and help ensure studies are conducted in accordance with study protocols, Good Clinical Practice (GCP), and applicable regulations. Previous clinical research experience is preferred but not required. We provide structured onboarding, hands-on training, direct mentorship, and opportunities for long-term professional and leadership development. Primary Responsibilities Leadership & Operations Conduct protocol-required physical examinations and clinical assessments. Review medical histories, medications, laboratory results, and study eligibility. Evaluate, document, and manage adverse events and participant safety concerns. Complete accurate clinical documentation and source records. Maintain clear communication regarding progress, concerns, risks, and next steps. Take ownership of assigned responsibilities and follow them through to completion. Collaborate with Principal Investigators, study coordinators, and sponsors to ensure protocol compliance. Participate in investigator meetings, sponsor visits, monitoring visits, and study training. Provide clinical guidance and mentorship to research coordinators and staff. Help develop clinical competencies across the research team. Promote a culture of accountability, ownership, teamwork, and continuous improvement. Follow study protocols, company SOPs, Good Clinical Practice (GCP), and all applicable regulatory requirements. Support initiatives that improve participant safety, data quality, and operational excellence. Qualifications Active, unrestricted California license as an NP, PA, MD, or DO. Graduate of an accredited Nurse Practitioner, Physician Assistant, Medical Doctor, or Doctor of Osteopathic Medicine program. Current board certification, as applicable. Strong clinical assessment and decision-making skills. Excellent communication, organization, and documentation skills. Professional, dependable, detail-oriented, and eager to learn. Current BLS certification (or ability to obtain upon hire). Comfortable using electronic medical records and computer-based systems. Preferred Qualifications Previous clinical research experience. Good Clinical Practice (GCP) knowledge. ACLS certification. Bilingual in English and Spanish. Demonstrated leadership experience managing clinical research teams. Strong knowledge of FDA regulations, ICH-GCP, HIPAA, IRB requirements, and clinical research operations. Proficiency with CRIO or comparable Clinical Trial Management Systems. Strong analytical, organizational, communication, and leadership skills. Ability to prioritize effectively in a fast-paced environment. Nurse Practitioners, Physician Assistants, Medical Doctors, and Doctors of Osteopathic Medicine are encouraged to apply. Who Will Thrive in This Role We're looking for someone who: Thrives in a fast-paced, growing organization. Takes ownership and consistently follows through. Communicates proactively and maintains visibility regarding progress, challenges, and solutions. Enjoys learning and continuous improvement. Thinks critically and helps solve problems. Works collaboratively within a multidisciplinary team. Demonstrates professionalism, integrity, and sound clinical judgment. Builds trust with patients, physicians, sponsors, and colleagues. Values accountability, teamwork, and personal growth. Wants to grow into a clinical leadership role within an expanding research organization. What We Offer Structured clinical research onboarding and training. Direct mentorship from experienced Principal Investigators. Exposure to studies across multiple therapeutic areas. Ongoing coaching, feedback, and professional development. Collaborative, transparent, and team-oriented culture. Opportunities to advance into senior clinical and leadership positions. Health, dental, and vision insurance. Paid time off and paid holidays. Competitive compensation based on experience and qualifications. Equal Opportunity Employer Chemidox Clinical Trials is an Equal Opportunity Employer. Qualified applicants will receive consideration for employment without regard to any characteristic protected by applicable federal, state, or local law. How to Apply Please submit your resume along with a brief statement describing your interest in clinical research and your long-term professional goals.
Benefits:
401(k) Dental insurance Health insurance Life insurance Paid time off Vision insurance
