In-House Clinical Research Associate - Path to CRA Travel

Rho

Polska

On-site

PLN 120,000 - 180,000

Full time

32 hours ago
Be an early applicant

Get a reply from this employer

Your resume and cover letter, tailored to exactly what they’re hiring for.

Get past ATS filters

Benefits offered by this job

Flexibility

Job summary

Rho is hiring an In-House Clinical Research Associate to join our team in Poland. You will monitor trials, manage CTMS data, and support on-site and remote activities to ensure compliance with ICH/GCP guidelines.

You will collaborate with the Project Manager, traveling CRAs and Lead CRA to grow into a traveling CRA role, develop study plans, and maintain essential documents across sites.

Qualifications

  • Bachelor's degree in life science, nursing or pharmacy.
  • Understanding of regulatory and ethics submission processes; ICH GCP familiarity.
  • Desire to grow into traveling CRA role.
  • Strong communication skills; fluent in English and local language.
  • Commitment to quality and collaborative culture.
  • Ability to adapt in a dynamic CRO environment.

Responsibilities

  • Collect, track and review site records relating to screening and enrollment.
  • Assist in the development of study plans and status reports; maintain regulatory documents.
  • Interact with sites, clients, vendors and internal study team members.
  • Maintain the clinical trials management system (CTMS) and other project tracking tools.
  • Assist with data review and query resolution; co-monitoring on-site and remotely.
  • Coordinate TMF audits and on-site monitoring activities.

Skills

Strong communicator
Fluency in English
Attention to detail
CRO environment knowledge
Project coordination

Education

Bachelor's degree in life science / nursing / pharmacy

Tools

CTMS
Project tracking tools

Job description

Rho is hiring an In-House Clinical Research Associate to join our team in Poland. You will monitor trials, manage CTMS data, and support on-site and remote activities to ensure compliance with ICH/GCP guidelines.

You will collaborate with the Project Manager, traveling CRAs and Lead CRA to grow into a traveling CRA role, develop study plans, and maintain essential documents across sites.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

In-House Clinical Research Associate
In-House Clinical Research Associate

Rho • Polska

On-site
PLN 120,000 - 180,000
Flexibility
Remote Oncology CRA II / Senior CRA
Remote Oncology CRA II / Senior CRA

Precision Medicine Group • Polska

Hybrid
PLN 120,000 - 180,000
Restaurant d'entreprise
Indemnités de stage/alternance
Clinical Research Associate
Clinical Research Associate

Axcellant • Polska

Hybrid
PLN 120,000 - 180,000
Flexible working model
Competitive compensation
Senior CRA II - Home-Based Oncology Monitoring (Poland)
Senior CRA II - Home-Based Oncology Monitoring (Poland)

Precision Medicine Group • Polska

Hybrid
PLN 120,000 - 180,000
Clinical Research Associate – Poland
Clinical Research Associate – Poland

BiTrial • Polska

Hybrid
PLN 120,000 - 180,000
Senior Oncology CRA — Remote Poland
Senior Oncology CRA — Remote Poland

Precision for Medicine • Polska

Hybrid
PLN 120,000 - 180,000
Clinical Research Associate - Poland (Remote/Hybrid)
Clinical Research Associate - Poland (Remote/Hybrid)

Axcellant • Polska

Hybrid
PLN 120,000 - 180,000
Flexible working model
Competitive compensation
Senior CRA – Remote/Home-based Poland, Oncology Trials
Senior CRA – Remote/Home-based Poland, Oncology Trials

Precision Medicine Group (New York, United States) • Województwo mazowieckie

Remote
PLN 120,000 - 180,000
Senior Oncology CRA – Remote/Home-Based (Poland)
Senior Oncology CRA – Remote/Home-Based (Poland)

Precision for Medicine • Województwo mazowieckie

Remote
PLN 70,000 - 100,000
Senior CRA II - Oncology (Remote, Poland)
Senior CRA II - Oncology (Remote, Poland)

Precision Medicine Group, LLC. • Polska

Hybrid
PLN 120,000 - 180,000
Top locations