Senior CRA Medical Devices, Poland

IQVIA; Poland; Hybrid; PLN 255,000 - 341,000; Full time

Job summary

A leading global contract research organization is seeking a MedTech Senior CRA in Poland. You will be responsible for site selection, monitoring, and regulatory compliance in clinical trials. The ideal candidate has a background in life sciences and at least 3 years of experience in on-site monitoring. Strong communication skills and flexibility to travel are essential. A supportive work environment offers resources for career growth and flexible schedules.

Benefits

Home-office

Company car

Career growth resources

Qualifications

• Minimum of 3 years of on-site monitoring experience.
• Strong experience in monitoring of clinical trials.
• Ideally experience in Cardiology and/or Medical Devices trials.

Responsibilities

• Performing site selection, initiation, monitoring and close-out visits.
• Supporting the development of a subject recruitment plan.
• Collaborating with experts at study sites and with client representatives.

Skills

On-site monitoring experience

Strong communication skills

Attention to detail

Knowledge of GCP and ICH guidelines

Flexibility to travel

Bilingual in Polish and English

Education

University Degree in life science or health care

Job description

Are you interested in collaborating with leading medical device companies to help patients all around the world?

When you join IQVIA as a MedTech Senior CRA in Poland, you’ll enjoy the stability and resources of a leading, global contract research organization. With access to world-class training and mentoring, you’ll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.

Your responsibilities will include:

• Performing site selection, initiation, monitoring and close-out visits
• Supporting the development of a subject recruitment plan
• Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines; ISO14155
• Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
• Collaborating with experts at study sites and with client representatives
• Depending on client model there might be remote-monitoring, involvement in study start-up processes, specialisation on therapeutic area (medical devices)

Qualifications:

• University Degree in life science or other scientific discipline or apprenticeship in health care
• Minimum of 3 years of on-site monitoring experience, alternatively an equivalent combination of education, training and experience
• Strong experience in monitoring of clinical trials
• Ideally experience in Cardiology and/or Medical Devices trials
• Knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines, ISO14155
• Strong written and verbal communication skills, attention to detail and ability to work in a fast pace environment
• Good command of Polish and English language
• Flexibility to travel across Poland

What you can expect:

• Resources that promote your career growth
• Leaders that support flexible work schedules
• Programs to help you build your therapeutic knowledge
• Dynamic work environments that expose you to new experiences
• Home-office, company car, and more

Whatever your career goals, we are here to ensure you get there!

We invite you to join IQVIA.

Please apply with your English CV.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com