Principal Investigator (3219)
Company: Dm Clinical Research Group
Location: North Houston
Posted on: April 1, 2026
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Job Description:
Description The Principal Investigator (MD) 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. Assuming responsibility for the conduct of clinical
investigation protocols. Possessing a thorough understanding of the
requirements of each protocol. Determining adequate resources
available to conduct research protocols. Managing the medical care
of subjects; protecting the rights and welfare of subjects.
Ensuring the validity of the trial data reported to the sponsor.
Ensuring documentation of study-related procedures, processes, and
events. Ensuring the proper use and storage of Investigational
Products. Attending investigator meetings as necessary for study
participation. Assist with creating PI oversight plans for every
study. Conduct and oversee ongoing staff training. Conduct patient
consent discussions and ensure comprehension of medical procedures,
risks, benefits, and alternatives Provide clear explanations of
study protocols and ensure patients' understanding before obtaining
their consent Facilitate effective communication between patients,
healthcare providers, and research staff Any other matters as
assigned by management KNOWLEDGE & EXPERIENCE Education: Minimum
qualifications include an M.D or D.O with an active medical license
(medical license must be valid in the state in which the research
is conducted). Experience: At least 2 years of experience as a
Clinical Research Investigator Credentials: Medical licensure
(license must be valid in the state in which the research is
conducted). Board certification or board eligibility in a specialty
appropriate to the type of research being conducted at the site.
Training and certification in DMCR required training and Standard
Operating Procedures (SOP’s). Training and certification in Good
Clinical Practice (GCP) Knowledge and Skills: 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.
Keywords: Dm Clinical Research Group, Baytown , Principal Investigator (3219), Healthcare , North Houston, Texas
