Join our Talent Pool - Clinical Research Associates (Europe)

1 hour, 58 minutes ago
Full-time
Junior
Operations
Alimentiv

Alimentiv

Alimentiv specializes in providing comprehensive clinical research services for gastrointestinal and liver diseases, leveraging a global site network, advanced medical imaging, and biomarker discovery to enhance patient recruitment and accelerate clini...

Professional Services
251-1K
Founded 1986

Description

  • Support or conduct site management through remote and supervised onsite visits, including initiation, monitoring, and close-out.
  • Perform remote data and system reviews in EDC, CTMS, RBM, and TMF to ensure data quality, completeness, and regulatory compliance.
  • Assist or lead query resolution, safety reviews, and adverse event follow-up throughout the study lifecycle.
  • Support site startup and activation activities, including investigator coordination, trial material delivery, and recruitment support.
  • Maintain accurate, timely, and complete TMF documentation and request updates as needed.
  • Provide day-to-day operational support to Senior CRAs and Lead CRAs.
  • Participate in training, study meetings, and CRA development activities to build role competencies.
  • For senior roles, act as a subject matter expert, mentor, coach, and performance feedback resource for peers.
  • For senior roles, assist with selection, hiring, training, and supervision of CRAs as needed.
  • For senior roles, may serve as Lead CRA and manage monitoring services for projects or CRAs on large or complex studies.

Requirements

  • CRA I: minimum 1 year of experience plus an Honours Bachelor Degree.
  • CRA II: minimum 2 years of experience plus an Honours Bachelor Degree.
  • Senior CRA: minimum 3 years of experience plus an Honours Bachelor Degree.
  • Experience requirements may vary depending on role needs and seniority level.
  • Ability to support remote and onsite clinical monitoring activities across Europe.
  • Knowledge of SOPs, protocol requirements, and GCP.
  • Familiarity with clinical trial systems such as EDC, CTMS, RBM, and TMF.
  • Experience in site management, monitoring, query resolution, and safety review processes.
  • For senior roles, experience providing mentorship, training, supervision, or escalation support is preferred.

Benefits

  • Full-time, permanent employment.
  • Remote work arrangement.
  • Base salary with eligibility for a performance-based bonus.
  • Health benefits.
  • Dental benefits.
  • RRSP matching.
  • Additional total rewards offered.
  • Opportunity to join a talent pool for future openings across multiple seniority levels.

Interested in this position?

Apply directly on the company website

Apply Now

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