Sub Investigator (Non MD) (4501)

Dm Clinical Research Group; Phoenix (AZ); On-site; USD 90,000 - 130,000; Full time

Job summary

DM Clinical Research Group in Phoenix, AZ seeks a Sub-Investigator (Physician Assistant or Nurse Practitioner) to ensure protocol adherence and protect subject welfare, directing trial conduct per FDA/ICH guidelines.

Responsibilities include clinical safety assessments, training, maintaining licensure, supervising clinical staff, documenting procedures, and attending investigator meetings as needed.

Qualifications

• Bachelor's or Master's in Nursing required.
• Current nursing licensure in good standing (PA or NP).
• Previous clinical research experience required.
• English and Spanish language skills preferred.

Responsibilities

• Complete DMCR training, including GCP and IATA.
• Maintain up-to-date curriculum vitae and current licensure to practice.
• Assist in managing the clinical staff at the site.
• Perform clinical-related procedures and trial-related decisions delegated by the PI.
• Perform clinical safety assessments and monitoring for trial participation.

Skills

Clinical research knowledge

Nursing skills

Communication skills

Bi-lingual English/Spanish

Diagnostic skills

Education

Bachelor's or Master's in Nursing

Job description

Job Details: Job Location: Phoenix - Phoenix, AZ, Salary Range: Undisclosed, 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.

Qualifications: