Sub Investigator (NP)

Dm Clinical Research Group; Houston (TX); On-site; USD 110,000 - 150,000; Full time

Job summary

Dm Clinical Research Group seeks a Sub-Investigator (Nurse Practitioner) to ensure protocol adherence, protect subject welfare, and oversee data integrity at the Houston site. The role involves clinical procedures, staff coordination, and regulatory compliance under Principal Investigator supervision.

The ideal candidate holds a nursing degree (BSN/MSN) with clinical research experience and strong communication skills in English, with bilingual English/Spanish proficiency preferred.

Qualifications

• Strong nursing clinical skills and patient care.
• Experience in clinical research contexts.
• Excellent written and verbal communication in English.

Responsibilities

• Ensure adherence to protocol and safeguard human subjects.
• Maintain current nursing licensure and CPR/ACLS as applicable.
• Coordinate clinical staff activities and site operations.
• Conduct safety assessments and trial-related procedures (e.g., vitals, EKGs, phlebotomy).
• Document study procedures and events accurately.

Skills

Nursing skills

Clinical research knowledge

Communication skills

English proficient

Bilingual English/Spanish

Education

Bachelor's or Master's in Nursing

Job description

The Sub-Investigator (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 & RESPONSIBILITIESCompleting 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 evaluationPossessing 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 managementKNOWLEDGE & EXPERIENCEEducation:Bachelors or Masters in NursingExperience:Previous clinical research experienceNursing experience in a clinical settingCredentials:Current nursing licensure in good standing (Physician Assistant or Nurse Practitioner)Knowledge and Skills:Basic clinical and patient care skillsKnowledge of nursing and medical principles and techniquesClinical research knowledgeStrong communication skills, both written and verbalStrong diagnostic skillsEthical and legal healthcare principles in patient careProficient 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.