Start-up Specialist, Phase I

Fortrea•Durham, NC

6d•Remote

About The Position

Our CPS team is currently seeking a Study Start Up Specialist with 2+ years of start-up experience residing with the U.S. This role serves as the primary contact with investigative sites during site start-up activities and maintenance. The specialist is responsible for collecting the required investigator and essential documents for a study to ensure EC/IRB/Third body/Regulatory Authority and any other local applications are made within the agreed timelines. The role ensures that documentation meets the specifications required by applicable regulations and sponsors. The specialist proactively interacts with EC/IRB/Third body/Regulatory Authorities to provide guidance regarding requirements and maintains awareness of current regulatory standards related to submissions. This position serves as a local expert in project start-up activities for a particular country or region and may act as a knowledge resource to mentor and train new hires and less-experienced department colleagues.

Requirements

University/College degree (life science preferred), or certification in a related allied health profession from an appropriate accredited institution (e.g., nursing certification, medical or laboratory technology)
2 years' work experience in clinical research, including a strong working knowledge of the ICH guidelines and RA, IRB/IEC regulations.
High School Diploma or equivalent AND a minimum of 2 years' work experience in clinical research, including a strong working knowledge of the ICH guidelines and RA, IRB/IEC regulations will be considered.
Minimum of 2 years of experience in clinical development or start-up/ regulatory process.
Working knowledge of ICH, RA, IRB/IEC, and other applicable regulations/guidelines; familiarity with investigator start-up documents and contract/budgets negotiation process; previous interaction with operational project teams and investigative sites.
Demonstrated understanding of research protocol requirements and proven ability to communicate them/educate others about them.
Comfortable working in a fast-paced environment where no deviations from the study protocol are allowed, and not meeting a timeline for even few minutes will create a quality issue.
Ability to adapt to changing priorities constantly.
Teamwork and people skills are essential.
Comfortable working in a technology-based environment where data is collected directly into an electronic environment.
Ability to sit for extended periods and operate a vehicle safely.
Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
Regular and consistent attendance.

Nice To Haves

Life science preferred degree

Responsibilities

Maintain awareness of regulatory legislation, guidance, and practice in the assigned countries.
Coordinate, collect and organize data and information required by EC/IRB/Third body/Regulatory Authority including but not limited to the preparation of study documentation such as the country application form and cover letter for sponsor review as applicable.
Compile and prepare routine submission filed to IRB/IEC/Third body/Regulatory Authorities (e.g., INDs/CTAs) and liaise with them as applicable regarding submission/approval.
Liaise with internal and external vendors in the generation of Regulatory Authority submissions (as applicable).
Perform a review of final submission documents as applicable.
Ensure that all assigned start-up and maintenance activities are on track, in accordance with client expectations and budget and in compliance with applicable laws and guidelines, regulatory requirements, ICH/GCP, SOPs and quality standards.
Prevent and escalate study issues appropriately and in a timely fashion.
Perform other duties as assigned by management depending upon country and situational requirements with proper supervision [if applicable].
Serve as primary contact for investigative sites and ensure documents required are collected in a timely manner.
Collect and track all the necessary documents required and perform a quality review, formatting, and compilation of the final documents for effective and compliant site activation and maintenance without supervision.
Ensure high quality documents are filed and systems are updated on an ongoing and timely basis, making Fortrea ready for an audit at any time.
Participate in team and project meetings as applicable.
When needed, assist in the strategy definition for Site Activation and provide accurate projections and timelines to study teams.
Review and customize country and site-specific patient informed consent forms for compliance with local requirements and protocol.
Proactively resolve informed consent issues and other potential difficulties with study sites.
May support the negotiation of site contracts and budgets with sites, if applicable and track progress of contract and budget milestones/developments, intervening and escalating as appropriate.
Proactively identifying and escalating to Submission Leads any risk to meeting deliverables.
Notify the Submissions Lead of hours identified as Out-of-Scope or overburn.
Performs all other duties as needed or assigned.