FSP Sr CRA I - NY, NJ, PA

Fortrea; New York (NY); Remote; USD 115,000 - 120,000; Full time

Job summary

Fortrea seeks an experienced FSP Sr Clinical Research Associate to join their team in New York, New Jersey, or Pennsylvania. The role involves high-standard patient care in clinical trials focusing on oncology and CNS, offering a full-time opportunity with comprehensive benefits. Candidates must be adaptable and possess over 3 years of monitoring experience, emphasizing teamwork and technology utilization.

Benefits

Medical, Dental, Vision, Life Insurance

401(K)

Paid Time Off (PTO)

Employee recognition awards

Multiple Employee Resource Groups (ERGs)

Qualifications

• 3+ years of Clinical Monitoring experience required.
• Comfortable working in fast-paced and changing environments.
• Degree or certification in a related health profession preferred.

Responsibilities

• Responsible for site monitoring, study file maintenance, and close-outs.
• Ensure adherence to informed consent and regulatory requirements.
• Perform CRF review and query generation as assigned.

Skills

Clinical Monitoring

Oncology experience

CNS experience

Teamwork

Adaptability

Education

University or college degree

Job description

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Join to apply for the FSP Sr CRA I - NY, NJ, PA role at Fortrea

We are currently seeking Experienced Sr. CRAs with over 3 years of monitoring, to lead and support our FSP team! We are open to experienced CRAs in New York, New Jersey & Pennsylvania. Oncology & CNS experience ideal.

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)
• 3+ years of Clinical Monitoring experience
• Open to major hub locations in the Northeast US
  
  

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.
  
  

What do you get?

Benefits

Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including but not limited to:

• Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)
• 401(K)
• Paid time off (PTO) – Flex Plan
• Employee recognition awards
• Multiple ERG’s (employee resource groups)
• Target Pay Range (based on title): $115-120K
  
  

- Remote

Applications will be accepted on an ongoing basis.

Learn more about our EEO & Accommodations request here.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

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