Clinical Research Physician

Location Gdynia
Discipline: Clinical Development, Medical & Pharmacovigilance
Job type: Permanent
Contact name: Joe Pearce

Contact email:
Contact phone: +44 1293 584 300
Job ref: CRP Poland
Published: 29 days ago
Expiry date: 25 Apr 2024 23:59

  • Job Title: Clinical Research Physician

  • Location: On-site in Gdynia, Poland

  • Salary: Up to 270,000PLN (depending on experience)

  • Company: Global CRO


In this position you will conduct all clinical trials (studies) according to ICH GCP, local regulations, study protocol and company processes ensuring the medical wellbeing and safety of the participants through the safe performance and execution of the studies. You will drive clinical oversight and quality of the studies at site, or with PI oversight at other sites. You will proactively participate and engage in driving delivery of study targets, thereby contributing to the commercial success of the site which includes: recruitment, enrolment and retention of study participants.

Key Responsibilities

  • Carries out clinical evaluation and assessment of participants to ensure eligible participants are recruited and monitored for safety and adherence.

  • Attends Site Initiation Visits (SIV), Pre-Selections Visits (PSV) and Investigator meetings as required.

  • Participates in recruitment initiatives and strategy development to ensure targets are achieved; ensuring recruiting studies enroll according to plan within timelines and targets.

  • Reviews enrolment progress, pre-screening and screening success rates, screen failure rates, safety and retention of participants.

  • Interprets protocols and IB.

  • Manages and reviews IVRS, CRF/EDC, if applicable.

  • Oversees management of investigational medical product (IMP).

  • Oversees multiple studies and/or studies with higher numbers.

  • Completes documentation for PI handover.

  • Cares for and protects the safety of participants through ethical conduct; this should receive the highest priority at all times during all aspects of the study.

  • Fulfills and complies with all medical duties, ensuring that clinical trials are performed to acceptable medical, scientific and ethical standards and meet the - requirements as per protocol, SOP/COP ICH and local GCP guidelines and regulations.

To apply:

If you would like to discuss this vacancy further or to discuss your career options in confidence, please telephone on +44 (0) 1273 049 215

Please click ‘apply’ or contact Joe Pearce for any further information

About RBW Consulting

RBW Consulting is a life sciences talent & strategic consultancy with purpose, delivered through what we call Human Intelligence. We help life sciences businesses change the world by giving them the people, insight & networks to innovate and scale. We are proud of our role in helping companies deliver better health and wellbeing outcomes for patients We give back by playing an active role in funding initiatives that change lives We’ve created a culture rooted in support, transparency and mutual commitment. We lead with our values from the inside; empowering and investing in our people is more important than short-term commercial gain.

We are an equal opportunities Recruitment Business and Agency

RBW Consulting is an equal opportunity workplace. We prioritize talent (both current and potential) over resumes, challenge the status quo, and value people as our most important asset. We do not discriminate on the basis of race, ethnicity, colour, sex, gender identity or expression, sexual orientation, religion, age, marital status, visible or invisible disability, medical condition, national origin, veteran status, or any other protected status. We strive to be a diverse workforce that is representative at all levels and are committed to building a team that represents a variety of backgrounds, perspectives, and skills.