FSP Clinical Research Associate 2 - East Coast - Oncology

Fortrea; Massachusetts; Híbrido; USD 100 000 - 112 000; Tempo integral

Resumo da oferta

Fortrea on the East Coast is seeking a CRA 2 with 2 years of monitoring experience to support oncology trials. The role combines on-site and remote work, averaging 8–10 days on site each month, with travel to trial sites.

You will conduct monitoring visits, manage study documentation, verify consent and data accuracy, and assist with training. The position requires a degree or nursing licensure and is oriented toward a fast-paced, collaborative environment with travel both domestically and

Qualificações

• University degree or nursing licensure from an accredited institution.
• At least 2 years of clinical monitoring experience.
• 60% overnight travel required.

Responsabilidades

• Monitor clinical sites including routine visits and close-out, maintain source data and study files.
• Manage site activities per project plans and coordinate with vendors.
• Perform on-site monitoring and ensure proper materials for protocol entry.
• Ensure informed consent procedures and protocol compliance.
• Review CRFs and detect data issues; support SAE reporting.
• Assist training and coordinate local project activities as needed.
• Travel as required to sites; work in a fast-paced environment.

Conhecimentos

2 years monitoring experience

oncology experience

Formação académica

University degree or nursing licensure

Descrição da oferta de emprego

Our FSP team is currently seeking a CRA 2 with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote. Seeking candidates on the East Coast with oncology experience.

What You Will Do

You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situations based upon clinical research standards.

Responsibilities

• Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -
• Responsible for all aspects of site management as prescribed in the project plans
• General On-Site Monitoring
• Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study
• Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements
• Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data
• Responsible for all aspects of registry management as prescribed in the project plans - Undertake feasibility work when requested
• Complete Serious Adverse Event (SAE) reporting, process production of repo11s, narratives and follow up of SAEs
• Independently perform CRF review; query generation and resolution against established data review guidelines on Fortrea or client data management systems as assigned by management
• Assist with training of new employees, eg. co-monitoring
• Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable) and may act as a local client contact as assigned
• Perform other duties as assigned by management

Requirements

• University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure)
• 2 years of Clinical Monitoring experience
• 60% overnight travel

The important thing for us is you are comfortable working in an environment that is:

• Fast paced: where no deviations from the study protocol are allowed, and not meeting a timeline for even few minutes will create a quality issue.
• Changing priorities constantly asking you to prioritize and adapt on the spot.
• Teamwork and people skills are essential for the study to run smoothly.
• Technology based. We collect our data directly into an electronic environment.

Work Environment

• Work is performed in an office environment with exposure to electrical office equipment.
• Frequent travel to clients/ site locations with occasional travel both domestic and international.

Physical Requirements

• 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.
• Varied hours may be required.
• Target Pay Range: $100-112K

- Remote

Applications will be accepted on an ongoing basis.

Learn more about our EEO & Accommodations request here.