Clinical Sub-Investigator (Nurse Practitioner) Job at Hope Biosciences Research Foundation, Sugar Land, TX

eHo5TXZZalhxZ1lrcVdrVzNhd1M3c2F1
  • Hope Biosciences Research Foundation
  • Sugar Land, TX

Job Description

About Us

Hope Biosciences Research Foundation is dedicated to advancing medical science by researching the potential of regenerative medicine. We are committed to conducting high-quality clinical trials across various therapeutic areas, starting with areas of unmet need.

Job Summary

We are seeking a skilled and dedicated Clinical Sub-Investigator to join our clinical research team. As a Clinical Sub-Investigator, you will play a critical role in the execution of clinical trials, contributing to the development of new therapies and medical advancements. You will be 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.

Key Responsibilities

  • Patient Screening : Screen and evaluate potential study participants for eligibility based on protocol criteria.
  • Informed Consent: Obtain informed consent from eligible participants, ensuring that they fully understand the study and their rights.
  • Clinical Assessments : Perform medical assessments, physical examinations, and other clinical procedures as required by the study protocol, such as phlebotomy, intravenous infusions, and lab work evaluation.
  • Data Collection : Accurately collect, record, and maintain clinical trial data, adhering to regulatory and quality standards.
  • Safety Monitoring : Monitor and report any adverse events or side effects experienced by study participants. Perform clinical-related procedures and/or make important trial-related decisions delegated by the Principal Investigator.
  • Compliance : Ensure strict adherence to Good Clinical Practice (GCP), local regulations, and ethical standards throughout the study. Manage the activities and performance of the clinical site staff.
  • Collaboration : Collaborate closely with the Principal Investigator, study coordinators, and other team members to coordinate and manage the study activities.
  • Protocol Adherence : Possess a thorough understanding of the requirements of each study protocol and implement all study procedures as outlined.
  • Study Documentation : Create, maintain, and organize study documentation, including study files, source documents, case report forms, organizational SOPs, and guidance documents. Ensure all essential documents, including Investigator Site File (ISF) are accurate and up to date.
  • Communication : Provide clear and timely communication with study participants, sponsors, and regulatory authorities as required.
  • Education : Stay updated on relevant clinical research developments and participate in continuing education opportunities to enhance your clinical knowledge and skills.
  • Any other matters as assigned by management.

Qualifications

  • PA ( Physician Assistant) or NP (Nurse Practitioner)
  • Current nursing licensure in good standing
  • 2+ years of previous clinical research experience
  • Strong understanding of GCP and ICH guidelines
  • Strong interpersonal and communication skills, both written and verbal
  • Attention to detail, the ability to work independently, and as part of a team
  • Proficient in medical record-keeping and data management

Pay

  • Competitive Market

Job Tags

Local area,

Similar Jobs

Glodom Language Solutions Co., Ltd.

Native Translator:English to German/French(Remote full-time) Job at Glodom Language Solutions Co., Ltd.

Requirements Native in German/French Degree in translation, interpretation, language studies, or related field Experience in translation, interpretation, localization Curious, quick learner (enjoy learning how things work), and attentive to details Flexible... 

TeamLogicIT

Help Desk Support and Level 1 Technician Job at TeamLogicIT

 ...defined processes to meet defined SLAs.~Use remote tools and diagnostic utilities to aid in resolving support requests.~Perform hands-on fixes at the desktop level when remote tools are not appropriate, including hardware repairs, delivery of peripherals, or other fixes... 

Ultimate Staffing

Regulatory Affairs Specialist Job at Ultimate Staffing

Position Overview Ultimate Staffing Services is actively seeking a dedicated Regulatory Affairs Specialist to join their client's team in Union, California. This position will play a crucial role in supporting the Regulatory Affairs department and the broader organization... 

H-E-B, Inc.

First Officer Job at H-E-B, Inc.

 ...safety culture. Once aboard, you will enjoy a fast paced, dynamic work environment with ample career development opportunities, coupled...  ...~2000 hours total time ~500 hours turbine (jet)~ FAA Airline Transport Pilot Certification (ATP)~ FAA First Class Medical Certificate... 

Accretional

Software Engineering Intern (AI/ML) Job at Accretional

 ...also offer: Hourly pay of $25/hr Networking and continuing education opportunities Paid trips to San Francisco for remote interns Lunch stipend for interns working onsite NOTE: As this is a summer 2025 internship role, applicants should be prepared to start...