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Assistant Cra 1 Jobs (NOW HIRING)

Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical ... CRA staff oversight lead. * May assist with the development and or review of study related ...

Clinical Research Assistant

Belmont, MA · On-site

$21.53 - $29.08/hr

The Neurobiology of Fear lab at McLean and Center for Suicide Research and Prevention at MGB/Harvard is seeking applications for 1 full-time Clinical Research Assistant (CRA) to coordinate and ...

The Position The Clinical Research Associate (CRA) provides support to Study Lead(s) in clinical ... Routinely monitor TMF inspection readiness for assigned studies * Assist Study Lead with ...

... * Assist the PM with the development of study related project plans and templates as per study ... • CRA II: Approximately 1-2 years of Clinical Research Associate experience or equivalent ...

May assist in monitoring visit preparation and/or follow up such as teleconference arrangements ... As one of the largest technology and professional staffing companies and one of the largest ...

... Assistant / In House CRA looking to become a CRA? 🔹 Do you already have 1-2 years of CRA experience and want to broaden your experience within a client-dedicated model? 🔹 Are you looking for a ...

... Assistant / In House CRA looking to become a CRA? 🔹 Do you already have 1-2 years of CRA experience and want to broaden your experience within a client-dedicated model? 🔹 Are you looking for a ...

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Assistant Cra 1 information

What are the most commonly searched types of Cra 1 jobs? The most popular types of Cra 1 jobs are:

Monitoring Excellence Academy - OMEA - Oncology / CAR T & Ophthalmology - CRA 1

Fortrea

Durham, NC • Remote

$80/hr

Other

Posted 18 days ago


Fortrea rating

7.2

Company rating: 7.2 out of 10

Based on 9 frontline employees who took The Breakroom Quiz

44th of 56 rated research


Job description

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 Ophthalmology 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, ifapplicable) 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 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.