Clinical Research Associate – Remote/Onsite Opportunities

Alimentiv

Warszawa

On-site

PLN 100,000 - 180,000

Full time

10 days ago
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Benefits offered by this job

Health benefits
RRSP matching
Bonus eligibility

Job summary

Alimentiv is building a talent pool for anticipated Clinical Research Associate needs across CRA I/II and Sr CRA roles, supporting its Clinical Monitoring team in a regulated environment. Roles include site management through remote and supervised onsite visits, data reviews (EDC/CTMS/RBM/TMF), query resolution, safety follow-up, site startup activities, and TMF documentation.

Involves collaboration with investigators and study teams, with career progression opportunities and ongoing CRA

Qualifications

  • CRA I - minimum 1 year experience + Honours Bachelor Degree
  • CRA II - Minimum 2 years experience + Honours Bachelor Degree
  • Sr. CRA - Minimum 3 years experience + Honours Bachelor Degree

Responsibilities

  • Support/site management through remote and supervised onsite visits per SOPs and GCP
  • Perform remote data/system reviews (EDC, CTMS, RBM, TMF) for data quality and compliance
  • Assist with 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, requesting updates as required
  • Provide day-to-day operational support to Senior CRA, and Lead CRAs
  • Participate in training, study meetings, and CRA development activities, building competencies required for role progression

Skills

Mentoring
Regulatory compliance
Site management
Remote monitoring

Education

Honours Bachelor Degree

Tools

EDC
CTMS
RBM
TMF

Job description

Alimentiv is building a talent pool for anticipated Clinical Research Associate needs across CRA I/II and Sr CRA roles, supporting its Clinical Monitoring team in a regulated environment. Roles include site management through remote and supervised onsite visits, data reviews (EDC/CTMS/RBM/TMF), query resolution, safety follow-up, site startup activities, and TMF documentation.

Involves collaboration with investigators and study teams, with career progression opportunities and ongoing CRA

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