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Job Details

CLINICAL RESEARCH ASSOCIATES /all levels/ office or home-based in Lithuania/ UP TO 5K EUR SIGN ON BONUS!

Company: Covance
Location: Lithuania
Reference: 44909BR
Closing Date: 15 Mar 17
Type: Permanent
Salary (£): Competitive
Benefits:

Job Summary:

Our mission - bringing medical miracles to market sooner - impacts the lives of millions of people all over the world. Our current growth of Clinical Development Services (CDS) in European countries brings new opportunities not only for clinical roles, but also another business functions.

Requirements:

At the moment we are looking for Clinical Research Associates on different levels – CRA I, CRA II and Senior CRAs in Lithuania (office or home based) - this is a great moment to join us ! - up to EUR 5000 Sign on Bonus!

As CRA you will be responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits.

Responsibilities:

  • Site administrating and site monitoring responsibility for clinical studies according to Standard Operating Procedures, ICH Guidelines and GCP;
  • Recruiting potential investigators, preparing EC submissions, translating study-related documentation, organizing of meetings and other tasks as instructed by supervisor;
  • Completing Serious Adverse Event (SAE) reporting, processing production of reports;
  • Negotiating study budgets with potential investigators and assisting the legal department with statements of agreements as assigned;
  • Interact with internal work groups to evaluate needs, resources and timelines;
  • Assist with training, mentoring, and development of junior employees, e.g. co-monitoring (for CRAs II);
  • Serve as lead monitor for a protocol or project and may assist in establishing monitoring plans as assigned (for CRAs II).

Required skills, experience and education:

  • Minimum 1 year of relevant clinical research Experience in pharmaceutical or CRO industries;
  • University Degree (life science) or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology);
  • Fluency in local and English language.
  • Understanding of the clinical trial process;
  • Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements;
  • Thorough knowledge of monitoring procedures.
  • In return, we offer you the opportunity to develop your career with an international organization; to pursue further training and to take advantage of our flexible conditions and attractive remuneration package.


Your rewards:

  • Up to a EUR 5,000 sign on bonus - limited time only, apply now!
  • The opportunity to pursue further training and an interesting career in an inspiring environment that values achievement, supports a balance between your personal and professional life and allows you to make meaningful contributions
  • Flexible conditions and an attractive remuneration package


THERE IS NO BETTER TIME TO JOIN US!

Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran). Your confidentiality and privacy are important to us.

 

Apply for this job: CLINICAL RESEARCH ASSOCIATES /all levels/ office or home-based in Lithuania/ UP TO 5K EUR SIGN ON BONUS!

Contact Information:

Address:  Covance- Warsaw


Poland
Tel: 
Fax: 
Website:  Visit Our Web Site

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