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Clinical Research Associate (all levels) with Oncology Experience
Labcorp
Place of work
Czech Republic
Czech Republic
Contract type
full-time
full-time
Information about the position
Job description, responsibilities and duties
Job Title: Clinical Research Associates
Job Code: 37715BR
Job Location: Regional, CZE
Clinical Research Associate
Job Description
Covance is one of the world's most dynamic drug development services companies, providing integrated, tailored solutions to the pharmaceutical and biotechnological industries.
We are currently looking for:
Clinical Research Associates (CRA) in Czech Republic with Oncology Experience .
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 Covance 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 Covance 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 and SCRAs);
- Serve as lead monitor for a protocol or project and may assist in establishing monitoring plans as assigned (for CRAs II and SCRAs).
Job Code: 37715BR
Job Location: Regional, CZE
Clinical Research Associate
Job Description
Covance is one of the world's most dynamic drug development services companies, providing integrated, tailored solutions to the pharmaceutical and biotechnological industries.
We are currently looking for:
Clinical Research Associates (CRA) in Czech Republic with Oncology Experience .
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 Covance 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 Covance 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 and SCRAs);
- Serve as lead monitor for a protocol or project and may assist in establishing monitoring plans as assigned (for CRAs II and SCRAs).
Employee perks, benefits
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.
Information about the selection process
For more information and to apply online visit www.covancecareers.com, quoting the appropriate reference number.
THERE IS NO BETTER TIME TO JOIN US!
Education/Qualifications *
Experience *
EEO Employer 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.
Regional, CZE
Regional, Czech Republic
Apply URL: http://jobsearch.covance.com/jobs/1143227-pdf.aspx
THERE IS NO BETTER TIME TO JOIN US!
Education/Qualifications *
Experience *
EEO Employer 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.
Regional, CZE
Regional, Czech Republic
Apply URL: http://jobsearch.covance.com/jobs/1143227-pdf.aspx
Requirements for the employee
Candidates with education suit the position
University education (Bachelor's degree)
Language skills
English - Upper intermediate (B2)
Personality requirements and skills
Required education, skills, Experience :
- 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 Czech and English language.
- Understanding of the clinical trial process;
- Minimum 2 years of relevant clinical research Experience in pharmaceutical or CRO industries;
- Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements;
- Thorough knowledge of monitoring procedures.
- 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 Czech and English language.
- Understanding of the clinical trial process;
- Minimum 2 years of relevant clinical research Experience in pharmaceutical or CRO industries;
- Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements;
- Thorough knowledge of monitoring procedures.
Advertiser
Brief description of the company
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ID: 2135410
Dátum zverejnenia: 12.6.2015
2015-06-12
lokalita: Czech Republic Pozícia: Chemical Lab Technician, Clinical Data Manager, Clinical Research Associate, Medical/Pharmaceutical Sales Representative Spoločnosť: Labcorp