Sponsor Perm Clinical Research Associates

Category: CRA
Job #: 10897
Utilization: 100%
Location: ET or CT Timezones in US
Job Type: Perm
Therapeutics: Oncology and/or Hema/Onc

Exciting opportunity alert! We’re looking for dedicated Clinical Research Associates to join an incredible Oncology Sponsor recognized globally as a leader in precision-targeted cancer therapies. This is a permanent position ideal for someone sincere, eager to collaborate as part of a team, and genuinely motivated to grow and learn in their career. If you’re passionate about making a real impact in oncology research and thrive in a supportive, innovative environment, this could be the perfect fit. To succeed in this role, you’ll need to be located in either the EST or CST time zones to align with the team’s workflow.

If you’re ready to take your CRA career to the next level and contribute to groundbreaking cancer treatments, apply today!

Job Responsibilities:
  • Act as the "Site Manager" ensuring relationship with site(s) are positive, issues are resolved quickly, and communications are strong across all verticals.
  • Assist with the development of study manuals, CRFs, monitoring standards, site study tools and other study materials as required.
  • Develop and implement site recruitment, selection and initiation plan.
  • Manage and drive patient recruitment and enrollment tracking.
  • Provide training to sites on the study protocol, study conduct, CRF completion and data management expectations.
  • Ensure essential document collection for completeness per regulatory requirements.
  • Serve as a liaison with Investigators, Institutions and sites to provide support during the conduct of the clinical trial and serve as a resource for protocol and procedures.
  • Demonstrate knowledge of on-site monitoring to ensure compliance with GCPs, study protocols, and SOPs.
    Manage one or multiple studies.
  • Monitor product supplies/accountability including proper storage, dispensation, and disposal.
  • Manage study completion activities including CRF collection, query resolution, record archiving and site closeout activities.
  • Review in-house data and study tables.
  • Mentor, coach and provide guidance to clinical staff as appropriate.
  • Supervise and train other employees as appropriate.
Job Qualifications:
  • Must have a minimum 3 years' recent experience as a fully dedicated Regional, Home-Based, Field Monitor for a CRO or Pharma
  • Must be located in the ET or CT Time Zones in the US, close to a major airport, and have travel flexibility
  • At least 1 year of experience monitoring Oncology and/or Hema/Oncology is required
  • Must have Early Phase through Phase 3 experience
  • T Cell and/or Gene/Cell Therapy experience is a plus
  • Experience with MediData RAVE and measurement/grading tools like RECIST is a plus
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