Top 5 House cra Jobs in Durham, Nc

FSP Clinical Research Associate 2 - West Coast & Texas
Fortrea —Durham, NC
- $100,000 - $112,000 a year
- Full-time
- Mid-level
- Office
- Travel
2d
FSP Sr. Clinical Research Associate II - NYC Metro or PHL - Onc
Fortrea —Durham, NC
- $125,000 - $140,000 a year
- Full-time
- Up to 50% travel
- 5 years
- Office
FSP Clinical Research Associate 2 - California or Colorado
Fortrea —Durham, NC
- $100,000 - $112,000 a year
- Full-time
- Mid-level
- Office
- Travel
2d
Senior Clinical Research Associate - CNS/Rare Disease - Midwest - Remote
Worldwide Clinical Trials —Research Triangle Park, NC
- Full-time
- Remote
- Nursing
- 5 years
- English
Staff Accountant
Hazen and Sawyer —Raleigh, NC
- Bachelor of Science
- Mid-level
- 3 years
- Paid holidays
- Disability insurance
Quick Apply

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FSP Sr. Clinical Research Associate II - NYC Metro or PHL - Onc
Fortrea —Durham, NC
University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure).
$125,000 - $140,000 a year

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FSP Clinical Research Associate 2 - West Coast & Texas

Fortrea -
Durham, NC

Apply Now

Job Details

Full-time
$100,000 - $112,000 a year
2 days ago

Qualifications

Computer skills

Full Job Description

Our FSP team is currently seeking a CRA 2 on the West Coast or in Texas with 2 years of monitoring! May consider states west of Texas. 8-10 days on site per month being a mix of onsite and remote.

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

Applications will be accepted on an ongoing basis.

Learn more about our EEO & Accommodations request here .

Apply Now

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house cra jobs in durham, nc

FSP Clinical Research Associate 2 - West Coast & Texas

FSP Sr. Clinical Research Associate II - NYC Metro or PHL - Onc

FSP Clinical Research Associate 2 - California or Colorado

Senior Clinical Research Associate - CNS/Rare Disease - Midwest - Remote

Staff Accountant

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