(Senior) Clinical Research Associate / Poland
International, rapidly growing CRO is seeking a talented (Senior) Clinical Research Associate. The new incumbent will be accountable for study site management including site selection, initiation, routine monitoring, close-out and maintenance of study files. CRA also ensures the quality and integrity of data, compliance with relevant SOPs and regulatory requirements and study completion on time and within budget.
Our Clients are a full service globally based Contract Research Organisation with in-depth experience of the most challenging therapeutic areas. They are seeking an experienced Clinical Research Associate, to come on board to assist with the monitoring of their growing portfolio of projects.
We are currently hiring for CRA and SCRA positions in different locations in Poland, all seniority levels, variety of Sponsors who are Top 10 Pharmaceutical Companies. Interesting studies, possibilities to adjust to your expectations as per clinical career development.
Providing your application will give you access to recent job openings.
Location: Poland
Type of Contract: Permanent, home-based or office-based
Seniority: Senior/Associate
Duties associated with the role include:
Review approved protocol and ensure qualification, initiation, monitoring and closeout visits for research sites are carried out in full compliance
Ensure overall integrity of study and adherence to guidelines, protocol and regulations
Complete monitoring reports and follow up letters, including providing the summaries of significant findings, deviations, deficiencies and recommended actions to secure compliance
Take an active role in the project team by providing feedback and suggestions for successful completion of the project
Coach and mentor less experienced CRAs to assist in their development and training
Requirements:
University degree in life sciences/pharmacy/biotechnology
At least 1 year of independent monitoring experience (including pre-study, initiation, routine monitoring and close-out visits) according to protocol monitoring guidelines, SOPs, GCP/ICH Guidelines
Computer competency
Fluent command of English
Ability to complete tasks in an accurate and timely manner
This is a really exciting opportunity to join a team dedicated to supporting the development of ground-breaking drugs.
We’re onboarding “best in class” candidates, so give us a chance to meet you!
NOTE:
By sending your personal data to KCR Placement in a broader extent than required by art. 22 (1) of the Polish Labor Code, you give KCR Placement your consent to the data processing for the purpose of ongoing recruitment process.
The consent can be withdrawn at any time. Withdrawal of consent does not affect the legality of the processing carried out prior to its withdrawal.
Dane kontatkowe:
Olga Ojkało
olga.ojkalo@kcrplacement.com
tel.: (+48) 695-801-068
