Monitoring Excellence Academy - OMEA - Oncology / CAR T & Alzheimer's - CRA 1
Lifelancer · United States
Skills in this posting
Extracted from the posting text by the instrument — the demand side, read literally.
The posting
Job Title: Monitoring Excellence Academy - OMEA - Oncology / CAR T & Alzheimer's - CRA 1
Job Location: Remote United States
Job Location Type: Remote
Job Contract Type: Full-time
Job Seniority Level
Fortrea’s Monitoring Excellence Academy is hiring!! We are seeking strong, Oncology or Ophthalmology Clinical Research Coordinators or Research Nurses with 2+ years of current experience. Must have 2+ years of Oncology, CAR T or Alzheimer's as a CRC or research nurse. Open to various hub locations around the US and French Speaking candidates in Montreal, Canada. Must be willing to travel 65-70%.
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
Requirements
University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure)
2+ years as a Study Coordinator or Research Nurse in specified therapeutic areas
Oncology experience is strongly desired ; CAR T a plus
60-70% 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: $80-90K
#LI - Remote
Applications will be accepted on an ongoing basis.
Learn more about our EEO & Accommodations request here.
This job is curated by Lifelancer .
Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains.
Please apply via Lifelancer platform to get connected to the application page and to find similar roles.
Originally posted on Himalayas
Excerpt from the original listing. The full, current text lives at the source. Read and apply there →
The PivotHop read
- What a clinical research coordinator actually earnsmedian, seniority, by country
- Alternative careers for a clinical research coordinatorevery measured route out
- All open clinical research coordinator rolesthe full board
Where these skills also reach
Adjacent occupations measured from the same postings — readiness is what a clinical research coordinator’s profile already covers.
- 11 open medical writer roles58% readiness from clinical research coordinator
- 25 open statistician roles30% readiness from clinical research coordinator
- 442 open executive assistant roles26% readiness from clinical research coordinator
- 58 open pharmacist roles26% readiness from clinical research coordinator
More clinical research coordinator roles
- Senior Clinical Data Manager - sponsor dedicated - oncologyLifelancer · United States
- Lead Clinical Research AssociatePSI CRO · Peru
- Sr. Clinical Research Associate (Australia)Alimentiv · Australia
- Clinical Trial Manager (LATAM)Precision Medicine Group · Argentina, Brazil, Mexico
- Clinical Research Associate 1ICON · United Kingdom
Backfilled listing, refreshed with the nightly scrape; the employer has not claimed it yet. Are you the employer? Claim this listing and it can be featured to the candidates whose skills already reach it, first month free.