Clinical Sub-Investigator — Nurse Practitioner

Dm Clinical Research Group

Tomball (TX)

On-site

USD 85,000 - 110,000

Full time

14 days+

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Job summary

DM Clinical Research Group in Tomball, TX is seeking a Sub-Investigator to ensure protocol adherence, protect participant welfare, and maintain data integrity under the supervision of the Principal Investigator.

The role requires nursing licensure and relevant clinical research experience. Responsibilities include clinical procedures, regulatory compliance, and collaboration with the site’s clinical staff.

Qualifications

  • Bachelor's or Master's in Nursing.
  • Previous clinical research experience.
  • Nursing experience in a clinical setting.
  • Knowledge of nursing and medical principles and techniques.
  • Clinical research knowledge.
  • Strong communication skills, both written and verbal.
  • Strong diagnostic skills.
  • Ethical and legal healthcare principles in patient care.
  • Proficient communication and comprehension in English; bilingual English/Spanish preferred.

Responsibilities

  • Completing DMCR-required training, including GCP and IATA.
  • Maintaining knowledge of current FDA regulations, GCP/ICH guidelines, SOPs, and study protocols.
  • Maintaining current nursing licensure to practice.
  • Assisting in managing the clinical staff at the site.
  • Performing clinical-related procedures and trial-related decisions delegated by the PI.
  • Performing clinical safety assessments and monitoring for study participation.
  • Managing the medical care of subjects and protecting their rights.
  • Ensuring documentation of procedures and events.
  • Attending investigator meetings as necessary.
  • Other matters as assigned by management.

Skills

Nursing knowledge
Clinical research knowledge
Communication skills
Bi-lingual EN/ES

Education

Bachelor's or Master's in Nursing

Job description

DM Clinical Research Group in Tomball, TX is seeking a Sub-Investigator to ensure protocol adherence, protect participant welfare, and maintain data integrity under the supervision of the Principal Investigator.

The role requires nursing licensure and relevant clinical research experience. Responsibilities include clinical procedures, regulatory compliance, and collaboration with the site’s clinical staff.

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