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Senior Clinical Research Associate

Remote: 
Full Remote
Contract: 
Experience: 
Mid-level (2-5 years)
Work from: 
European Union

Offer summary

Qualifications:

University degree in life sciences/pharmacy/biotechnology, At least 3 years of independent monitoring experience, Fluent command of English, Computer competency.

Key responsabilities:

  • Ensure study integrity and adherence to guidelines
  • Complete monitoring reports and provide summaries of findings
  • De-risk project activities effectively
  • Coach and mentor less experienced CRAs
KCR logo
KCR SME https://www.kcrcro.com/
501 - 1000 Employees
See more KCR offers

Job description

KCR is a clinical development solutions provider creating value for biotechnology and pharmaceutical organizations. Founded in 1997, our expert teams support clients with full-service clinical development capabilities across three main areas: Trial Execution, Consulting and Placement. KCR operates across North America, Europe, and Australia, with main office locations in Boston US, Berlin Germany, and Warsaw Poland. Our geographical coverage across 25+ countries, cutting-edge technical capabilities and tailored offerings allow for the optimized delivery of solutions to develop life-changing therapies. KCR offers access to an estimated population of 1.1 billion people. For more information visit www.kcrcro.com.


We see human behind every number


Senior Clinical Research Associate


Location: Poland (remote)


We are currently hiring for SCRA positions. It is a Sponsor dedicated role for the company which is one of the 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.


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 3 years 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.


At KCR we put our mission: WE SEE HUMAN BEHIND EVERY NUMBER into our actions, therefore we offer our Employees benefits that comply with national regulations and provide the coverage that best meets employee needs.


To show that you are appreciated in our team, while working at KCR you will be provided with:


  • 1 additional day off for your birthday;
  • Private medical healthcare;
  • Sport card;
  • Loyalty Bonus Program (anniversary awards or additional paid time off);
  • Additional days off during Christmas period;
  • Employee referral system;
  • Onboarding process and induction training to develop deep sector knowledge and complex skills;
  • Latest technology and the most advanced equipment and working tools;
  • An open culture based on slim processes, in an agile structure with a flat hierarchy and direct access to the Management to share ideas and implement change and continuous improvement;
  • Mentoring and training programs related to clinical trials, therapeutic areas, hard and soft skills.


Our Privacy Policy

Your data will be processed in accordance with KCR Group Privacy Policy. For more details click here: https://www.kcrcro.com/privacy-policy/#privacy.


Providing your personal data is voluntary, however, if you do not provide us with the necessary information, we will not be legally allowed to get in touch with you and consider your application. By sending application documents containing your personal data to a wider extent than required by provisions of the applicable laws, you are granting consent for the data to be processed for the purposes of the ongoing recruitment.

You may also agree to enable other employers within KCR Group to communicate with you about potential job opportunities that match your area of expertise and interests.

If you would like your candidacy to also be considered for future recruitments, please select an additional consent or add the following statement to your application documents: “I agree to the processing of my personal data for any future recruitments conducted by KCR and/or KCR affiliates for a period of up to 3 years”. Such consent may be placed in your CV or electronic correspondence addressed to your potential employer.

You may withdraw any consent at any time. Withdrawal of consent does not affect the legality of the processing carried out prior to its withdrawal.


Your personal data will be shared with KCR and/or KCR affiliate that you are pursuing, and that company will be considered a separate data controller of your personal data. A full list of KCR affiliates is available at: https://www.kcrcro.com/privacy-policy/#kcr-entities.


You can contact KCR Group Data Protection Officer at gdpr@kcrcro.com any time with any questions or concerns regarding how your personal data is processed.

KCR is an equal opportunity employer providing its staff with excellent opportunities to build dynamic, long-term careers.

Required profile

Experience

Level of experience: Mid-level (2-5 years)
Industry :
Pharmaceuticals
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Computer Literacy
  • Detail Oriented
  • Mentorship

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