Clinical Research Associate – Poland

BiTrial; Polska; Hybrid; PLN 120,000 - 180,000; Full time

Job summary

BiTrial in Poland is seeking a Clinical Research Associate (CRA) for a full-time or part-time hybrid role based in Poland. You will conduct monitoring visits, develop site relationships, and manage essential trial documentation.

The ideal candidate holds a health/life science degree, has 1 year CRA experience, and can travel regularly with excellent English communication. Independence and remote work are valued.

Qualifications

• University degree in a health or life science related field (preferably medical doctor or pharmacist).
• 1 year Experience as a CRA.
• Experience both drug and Medical Device studies is a plus.
• Knowledge of clinical trial Protocol and Research methodologies.
• Skills in Clinical Operations and monitoring site performance.
• Valid driving license.
• Excellent written and verbal communication skills in English.
• Demonstrated flexibility in schedule and willingness to travel on a regular basis.
• Ability to work independently and remotely.
• Detail-oriented and efficient in time management.
• Ability to respond quickly to changing demands and opportunities.

Responsibilities

• Conduct different types of monitoring visits (pre-study visits, site initiation visits, interim monitoring visits & close out visits).
• Develop and maintain site and investigator relationships to ensure clinical trials are managed efficiently
• Perform source document verification and prepare monitoring visit reports, including confirmation and follow-up letter
• Manage the study documentation and other essential trial related documents
• Support regulatory submissions to the Competent Authority
• Participate in Investigator selection/feasibility process

Skills

CRA experience

Drug studies

Medical device studies

Clinical trial protocols

Clinical Operations

Site monitoring

Driving license

English communication

Flexible schedule

Travel willingness

Independent work

Remote work

Time management

Detail-oriented

Adaptability

Education

University degree in health or life sciences

Job description

As a Clinical Research Associate (CRA) you will have the unique opportunity to have an exciting career in the field of drug and medical device development as part of an expanding team.

This is a full-time or part-time hybrid role for a CRA based inPoland.

Responsibilities

• Conduct different types of monitoring visits (pre-study visits, site initiation visits, interim monitoring visits & close out visits)
• Develop and maintain site and investigator relationships to ensure clinical trials are managed efficiently
• Perform source document verification and prepare monitoring visit reports, including confirmation and follow-up letter
• Manage the study documentation and other essential trial related documents
• Support regulatory submissions to the Competent Authority
• Participate in Investigator selection/feasibility process

Qualifications

• University degree in a health or life science related field (preferably medical doctor or pharmacist)
• 1 year Experience as a CRA
• Experience both drug and Medical Device studies is a plus
• Knowledge of clinical trial Protocol and Research methodologies
• Skills in Clinical Operations and monitoring site performance
• Valid driving license
• Excellent written and verbal communication skills in English
• Demonstrated flexibility in schedule and willingness to travel on a regular basis
• Ability to work independently and remotely
• Detail-oriented and efficient in time management
• Ability to respond quickly to changing demands and opportunities

At BiTrial, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. BiTrial is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment.