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Job detail

Sub Investigator (2745)

DM CLINICAL RESEARCH GROUP

Employer page
#Phlebotomy#Patient Care#Nurse Practitioner#FDA Regulations#SOPs#Clinical Research#GCP#Protocol Adherence#EKG
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#IATA
#ICH Guidelines
#Clinical Safety
OtherOn Site2-5 yrs$60 - $75 / HOURPosted 5 months agoCloses Jul 27

Location

Hoover, Alabama

Salary

$60 - $75 / HOUR

Quick overview

The Sub-Investigator is responsible for ensuring adherence to study protocols and protecting the rights and welfare of research subjects. Key duties include performing clinical procedures, safety assessments, and managing the medical care of participants.

Requirements summary

Candidates must hold a Bachelor's or Master's in Nursing and a current Nurse Practitioner license in good standing. Previous experience in clinical research and a clinical setting is required.

bachelor degreepostgraduate degreePatient CarePhlebotomyPhysical ExamsClinical ResearchGCPEnglish ProficiencyEKGDiagnostic SkillsSpanish ProficiencyFDA RegulationsMedical PrinciplesIATAClinical Safety Assessments

Job description

Job DetailsJob Location

  • Boston -
  • Brookline,
  • MA 02446Salary
  • Range: $60.00 - $75.00 HourlyThe Sub-Investigator (Part time/Contract) 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. This Sub-I position is poised to turn into a fulltime position for the right candidate. 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 (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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DM CLINICAL RESEARCH GROUP

DM CLINICAL RESEARCH GROUP logo

Hiring organization

DM CLINICAL RESEARCH GROUP

DM Clinical Research is a network of clinical trial investigator sites with headquarters based out of Houston, Texas. We are the link connecting pharmaceutical and research organizations to caring individuals seeking to power the advancement of medicine. We work with qualified...

Explore employer profile
IndustryBiotechnology Research
TypePrivately Held
Size501-1,000 employees
HQHouston, TX
Founded2006

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