Sub Investigator (2532)

Dm Clinical Research Group; Tomball (TX); On-site; USD 85,000 - 110,000; Full time

Job summary

DM Clinical Research Group in Tomball, TX is seeking a Sub-Investigator to ensure protocol adherence, protect participant welfare, and maintain data integrity under the supervision of the Principal Investigator.

The role requires nursing licensure and relevant clinical research experience. Responsibilities include clinical procedures, regulatory compliance, and collaboration with the site’s clinical staff.

Qualifications

• Bachelor's or Master's in Nursing.
• Previous clinical research experience.
• Nursing experience in a clinical setting.
• 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 in English; bilingual English/Spanish preferred.

Responsibilities

• Completing DMCR-required training, including GCP and IATA.
• Maintaining knowledge of current FDA regulations, GCP/ICH guidelines, SOPs, and study protocols.
• Maintaining current nursing licensure to practice.
• Assisting in managing the clinical staff at the site.
• Performing clinical-related procedures and trial-related decisions delegated by the PI.
• Performing clinical safety assessments and monitoring for study participation.
• Managing the medical care of subjects and protecting their rights.
• Ensuring documentation of procedures and events.
• Attending investigator meetings as necessary.
• Other matters as assigned by management.

Skills

Nursing knowledge

Clinical research knowledge

Communication skills

Bi-lingual EN/ES

Education

Bachelor's or Master's in Nursing

Job description

Job Location: Tomball 13406 - Tomball, TX 77375The Sub-Investigator 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 (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