Sub-Investigator (NP)

DM Clinical Research; Dallas (TX); On-site; USD 90,000 - 130,000; Full time

Job summary

DM Clinical Research is seeking a Sub-Investigator (Physician Assistant or Nurse Practitioner) to ensure protocol adherence, subject safety, data integrity, and regulatory compliance under the Principal Investigator's direction.

The role requires nursing licensure, active clinical experience, and ability to manage study-related procedures, communicate effectively, and coordinate with clinical staff to support ongoing trials.

Qualifications

• Basic clinical and patient care skills.
• Knowledge of nursing and medical principles and techniques.
• Clinical research knowledge is preferred.
• Strong written and verbal communication skills.
• Good diagnostic abilities and clinical judgment.
• Proficient in English; bilingual English/Spanish preferred.

Responsibilities

• Ensure protocol adherence and subject safety under supervision of the Principal Investigator.
• Maintain licensure and complete required trainings (GCP, IATA).
• Monitor and assess subjects, perform related procedures, and support study activities.
• Document study events and procedures accurately in the CRF and logs.
• Coordinate with clinical staff and attend investigator meetings as needed.
• Support compliance with FDA and GCP/ICH guidelines.

Skills

Clinical care

Medical knowledge

Clinical research knowledge

Communication skills

Diagnostic skills

English proficiency

Bilingual English/Spanish

Education

Nursing degree (BSN/MSN)

Job description

The Sub-Investigator (Physician Assistant or Nurse Practitioner) is accountable and responsible for ensuring adherence to protocol requirements, protecting the rights and welfare of subjects, assuring the integrity of subject generated data and directing the conduct of research according to federal and state regulations and guidance documents.

DUTIES & RESPONSIBILITIES

• Completing DMCR-required training, including GCP and IATA.
• Maintaining a working knowledge of current FDA regulations, GCP/ICH guidelines, organizational SOPs, guidance documents, and study protocols.
• Maintaining a current, up-to-date curriculum vitae and current licensure to practice.
• Assisting in managing the activities and performance of the clinical staff affiliated with the site.
• Performing clinical-related procedures and/or making important trial-related decisions delegated by the Principal Investigator.
• Performing clinical safety assessments and monitoring for study trial participation to include such items as: physical exams, EKGs, phlebotomy, and lab work evaluation
• Possessing a thorough understanding of the requirements of each protocol.
• Managing the medical care of subjects; protecting the rights and welfare of subjects.
• Ensuring documentation of study-related procedures, processes, and events.
• Attending investigator meetings as necessary for study participation.
• Any other matters as assigned by management

KNOWLEDGE & EXPERIENCE

Education:

• Bachelors or Masters in Nursing

Experience:

• Previous clinical research experience
• Nursing experience in a clinical setting

Credentials:

• Current nursing licensure in good standing (Physician Assistant or Nurse Practitioner)

Knowledge and Skills:

• Basic clinical and patient care skills
• 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 skills both verbal and written in the English language are required.
• Proficient Bi-lingual (English/Spanish) communication and comprehension skills both in verbal and written are preferred.