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Job Details

CLINICAL RESEARCH ASSOCIATES - ALL LEVELS / Latvia

Company: Covance
Location: Latvia
Reference: 46046BR
Closing Date: 10 Feb 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. .

Requirements:

At the moment we are looking for Clinical Research Associates in Latvia (home based; all levels)

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 within oncology;
  • 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.

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 / Latvia

Contact Information:

Address:  Covance- Warsaw


Poland
Tel: 
Fax: 
Website:  Visit Our Web Site

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