JobsNurse PractitionerDallasSub Investigator (Nurse Practitioner)
DM CLINICAL RESEARCH GROUP
Posted 3 days ago
Sub Investigator (Nurse Practitioner)
DM CLINICAL RESEARCH GROUP · Irving, Texas, United States
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In short
The Sub-Investigator is responsible for ensuring protocol adherence, protecting subject welfare, and maintaining data integrity according to federal and state regulations. They perform clinical procedures, monitor safety assessments, and manage the medical care of research subjects.
What they're looking for
MUST-HAVE SKILLS
ALSO MENTIONED
Candidates must hold a Bachelor's or Master's degree in Nursing and possess current licensure as a Nurse Practitioner or Physician Assistant. Previous clinical research experience and a strong understanding of FDA regulations and GCP guidelines are required.
About the employer
DM Clinical Research
20 years of innovation in medical research. Excellence in Patient Centricity. · hiring as DM CLINICAL RESEARCH GROUP
DM Clinical Research is a network of clinical trial investigator sites with headquarters based out of Houston, Texas.
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We are the link connecting pharmaceutical and research organizations to caring individuals seeking to power the advancement of medicine. We work with qualified physicians with a diverse range of specialties—including cardiology, endocrinology, pediatrics, rheumatology, pulmonology and family medicine—and have conducted a wide variety of studies with successful enrollment targets. Websites: http://www.dmclinical.com
- INDUSTRY
- Biotechnology Research
- COMPANY
- Privately Held
- FOUNDED
- 2006
- HEADQUARTERS
- Houston, TX
- SIZE
- 501-1,000
- OFFICES
- 17 on LinkedIn
KNOWN FOR
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Questions about this role
- Is this DM CLINICAL RESEARCH GROUP role remote?
- Tagged on site.
- Does it sponsor visas?
- Listed as no visa sponsorship.
- What experience does it ask for?
- Listed as 2-5 years.
The posting, in full
Job Details: Job Location: Dallas, TX - Irving, TX, 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:
▶ READ THE FULL POSTING▼ CLOSE THE FULL POSTING
Job Details: Job Location: Dallas, TX - Irving, TX, 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:
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