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

Industrials

251-1K (570)

Founded 1986

27 open positions

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Join our Talent Pool - Clinical Research Associates (Europe)

5 months ago

United Kingdom, Belgium, Poland, Romania, Germany

Full-time

Junior

Recruiter

Operations

GCP

Apply Now

Alimentiv

Professional Services

251-1K

Founded 1986

View All Jobs 27

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

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