Clinical Research Coordinator​/Clinical Research Nurse- Contractor

Join to apply for the Clinical Research Coordinator / Clinical Research Nurse
- Contractor role at Site Bridge Research, Inc.

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Join to apply for the Clinical Research Coordinator / Clinical Research Nurse
- Contractor role at Site Bridge Research, Inc.

Site Bridge Description

Founded in 2021, Site Bridge Research is a community-focused integrated research organization, building a national network of community practices to deliver world-class industry sponsored clinical research on time and on budget, accelerating time to market and product adoption in communities that are the most vulnerable and the hardest to reach. The Site Bridge network extends reach further into these communities to empower a broader set of patients with some of the highest unmet needs to take part in clinical research to improve health outcomes.

Site Bridge also helps with FDA diversity planning and building effective community engagement strategies.

Site Bridge Description

Founded in 2021, Site Bridge Research is a community-focused integrated research organization, building a national network of community practices to deliver world-class industry sponsored clinical research on time and on budget, accelerating time to market and product adoption in communities that are the most vulnerable and the hardest to reach. The Site Bridge network extends reach further into these communities to empower a broader set of patients with some of the highest unmet needs to take part in clinical research to improve health outcomes.

Site Bridge also helps with FDA diversity planning and building effective community engagement strategies.



Job Description

Clinical Research Coordinator / Clinical Research Nurse
- Contractor

The Clinical Research Coordinator (CRC) is a specialized research professional working with and under the direction of the Clinical Principal Investigator (PI) on multiple ongoing research studies. While the Principal Investigator is ultimately responsible for the clinical trial, the CRC is responsible for the facilitation and coordination of the daily clinical trial activities and plays a critical role in the conduct of the study.

The CRC works collaboratively with the entire site team, sponsors, and clinical monitors to ensure ICH/GCP compliance, site productivity, and timely completion of studies. In addition, and most importantly, this role represents our mission and vision by focusing on the trusted physician/patient partnership from start to finish for every clinical trial conducted at the site and is key in transforming clinical research for every participant.

The position will be responsible for specific clinical site activities to maintain the operational excellence required of clinical sites/staff involved in clinical studies and to assure compliance with protocol-specific procedures, data acquisition, and records management. This role will report to the Director, Clinical Site Development Operations and Study Management.

Location:
The position is located in Lufkin, TX and will be required to be on-site.

Job Type: This is an (1099) Independent Contractor position and is open to both part-time or full-time availability.

Responsibilities

• Ensure clinical study compliance with local and federal laws and regulations according to ICH/GCP Guidelines
• Ensure study feasibility assessments for contracted sponsor-initiated studies
• Assist the Clinical/Site Ops Leads on the set-up/start-up of research site to prepare for start-up and conduct of clinical trials
• Lead oversight of pre-study, site initiation, and close-out visits with sponsor or CRO
• Consult with Site Leads, sponsor, and CRO to determine the best recruitment practices for site and trials
• Track study activities to ensure compliance with standard operating procedures (SOPs), protocols, and all related local, state, and national regulatory and institutional policies
• Arrange screening and recruitment of potential study participants by scheduling visits to establish Informed Consent and perform intake assessments according to protocols
• Create and maintain all essential documents and records related to the study
• Act as a point of reference for study participants by answering questions and keeping them informed on the study’s progress
• Oversee and/or manage the inventory of equipment and supplies related to the study, including documentation, reporting of issues, and ordering clinical supplies as needed
• Communicate with laboratories and clinical investigators to ensure review and reporting of lab results and other clinical testing results
• Direct the request, collection, labeling, storage, or shipment of interventional products
• Ensure collection of specimens, questionnaire information, and input of data and patient information into electronic clinical systems
• Monitor the enrollment status of participants at the site for each specific…