Fortrea
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Sr CRA - Oncology - FSP - North East & Texas
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Fortrea 1 week ago Be among the first 25 applicants Join to apply for the
Sr CRA - Oncology - FSP - North East & Texas
role at
Fortrea We are currently seeking
Experienced Oncology CRAs
residing in the North East (NY, NJ, CT or PA), and Texas.
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 onsite Clinical Monitoring experience Oncology experience required Open to major hub locations in the Northeast US and Texas
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): $115-140K depending on job title
- 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 Referrals increase your chances of interviewing at Fortrea by 2x Get notified about new Senior Clinical Research Associate jobs in
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Sr CRA - Oncology - FSP - North East & Texas
role at
Fortrea 1 week ago Be among the first 25 applicants Join to apply for the
Sr CRA - Oncology - FSP - North East & Texas
role at
Fortrea We are currently seeking
Experienced Oncology CRAs
residing in the North East (NY, NJ, CT or PA), and Texas.
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 onsite Clinical Monitoring experience Oncology experience required Open to major hub locations in the Northeast US and Texas
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): $115-140K depending on job title
- 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 Referrals increase your chances of interviewing at Fortrea by 2x Get notified about new Senior Clinical Research Associate jobs in
Durham, NC . Associate Director/Director, Clinical Trial Manager
Clinical Innovation & Digital Solutions Lead
Raleigh, NC $148,000.00-$194,000.00 6 days ago Scientific Manager, COA Implementation, Patient Centered Solutions
Durham, NC $95,300.00-$237,500.00 8 minutes ago Senior Site Manager, Radiopharmaceutical - FSP
Open Rank Faculty/Associate Director for Translational Research
Open Rank Faculty/Associate Director for Basic Cancer Research
Durham, NC $59,829.00-$99,960.00 1 day ago Freelance Senior Clinical Research Associate
Freelance Senior Clinical Research Associate
Chapel Hill, NC $63,875.00-$75,100.00 1 day ago Chapel Hill, NC $51,985.00-$72,826.00 1 month ago Clinical Research Specialist, Senior - Duke Cancer Institute
Sr. Research Associate, Clinical Immunology
Chapel Hill, NC $63,875.00-$75,100.00 1 month ago Senior Clinical Research Associate - Diabetes - East Coast - Remote
Senior Clinical Research Associate - Diabetes - West Coast - Remote
Chapel Hill, NC $43,000.00-$53,000.00 2 days ago Senior Clinical Research Associate - CNS - Central - Remote
Clinical Research Associate, Obesity/Diabetes/GLP-1 (Full Service) - IQVIA
Senior Clinical Research Associate - Obesity - Central
Senior Clinical Research Associate - CNS/Alzheimer's - Southeast - Remote
Post-Doc Research Associate - Dr. Nguyen's lab
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr