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Joboffer number #152398

CLINICAL RESEARCH ASSOCIATE WITH STRONG ONCOLOGY EXPERIENCE

CV Market´s client
Latvia
Job ad expired!

Job Description

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;
  • Serve as lead monitor for a protocol or project and may assist in establishing monitoring plans as assigned.


Requirements

Required skills, experience and education:

  • Minimum 2 years of relevant clinical research experience in pharmaceutical or CRO industries and minimum 1 year within oncology therapeutic area;
  • 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.


Company offers

We Offer:
Covance's ongoing success offers team members unsurpassed growth and career development opportunities.
At Covance, we help make the miracles of medicine a reality. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career.

There is no better time to join us!

For more information or to apply:
Please visit Covance career site at http://careers.covance.com/ quoting the appropriate reference number - 46046BR, or follow the link

Darba sludinājuma numurs
#152398

Location:
Latvia
Job type:
full-time
Additional info:
employee
Expiration date:
31 December 2014
Published:
01 December 2014

CV Market´s client

Covance is one of the world's most dynamic drug development services companies, providing integrated, tailored solutions to the pharmaceutical and biotechnological industries.

You can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world. Our commitment to this mission has resulted in Covance’s impressive history of company stability and growth.

For our CoSource department in Latvia we are currently looking for a home based:

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CLINICAL RESEARCH ASSOCIATE WITH STRONG ONCOLOGY EXPERIENCE
Employer is asking you to finalize your application on an external website. Please carefully follow further instructions. We hope you get the job!
Employer is asking you to finalize your application on an external website. Please carefully follow further instructions. We hope you get the job!