Sub Investigator (Non MD)

DM CLINICAL RESEARCH GROUP - 2.9

Albuquerque, NM Job Details 22 hours ago Qualifications Data integrity assurance Foreign language proficiency Direct patient care Nursing Management Healthcare staff management Patient monitoring Research ethical considerations EKG Writing skills Master's degree in nursing Care documentation Mid-level State healthcare regulations Patient safety Master's degree Data integrity and documentation ICH guidelines Collecting samples for laboratory testing Bachelor's degree Medical treatment knowledge Master of Nursing Managing clinical research teams Clinical documentation Research compliance clinical trial records management Advanced practice provider Clinical trial standard operating procedures Clinical trial patient safety management Implementing research protocols Bachelor's degree in nursing Full 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.