Job Title: Clinical Research Associates - All levels, Office /Home based
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Vacancy details
Vacancy description:
Job Code:
13644
Job Title:
Clinical Research Associates - All levels, Office /Home based
Job Category:
Clinical Research
Contract:
Permanent
Discipline:
CRA, Clinical Study Coordinator
Country:
Bulgaria, Czech Republic, France, Germany, Hungary, Italy, Netherlands, The, Poland, Romania, Russia, Spain, Switzerland, Ukraine, Serbia, United Kingdom
Location:
Berkshire, East Sussex
Min experience:
N/A
Annual salary:
Negotiable
Apply by:
06 Jun 2008
There are excellent opportunities around Europe for CRAs. Our client, a leading global CRO with a uniquely specialised therapeutic focus on CNS, Oncology and Pain, is seeking experienced CRAs at all levels, including SCRAs & Lead CRAs, in office or home/field based positions to monitor all types of clinical trials around Europe.
LOCATIONS: UK South-East - Maidenhead, Berkshire, Battle, East Sussex; Netherlands � Amsterdam; Germany � D�sseldorf; France � Paris; Spain � Barcelona; Switzerland � Zurich; Italy � Milan; Romania � Bucharest; Hungary � Budapest; Russia - Moscow, St Petersburg; Serbia � Belgrade; Ukraine � Kiev; Czech Republic � Prague; Bulgaria � Sofia; Poland � Warsaw
PRIMARY RESPONSIBILITIES include:
�Monitoring clinical trials ensuring adherence to GCP, investigator integrity, and compliance with all study procedures.
�Site management and performance (including documentation) according to ICH guidelines (country specific guidelines and government regulations), as well as FDA regulations (state and local laws), GCPs, and SOPs.
�Site management activities include all in house and on-site monitoring for all visit types.
�Participation in training programmes and mentoring new or less experienced team members.
�May be assigned as a Clinical Team Leader (CTA) responsible for managing specific clinical activities as assigned
QUALIFICATIONS, KNOWLEDGE & EXPERIENCE:
�BA/BS degree in the science/health care field, nursing degree, or equivalent
�High level of clinical research field monitoring experience in a CRO or Pharmaceutical/Biotech environment.
�In depth knowledge of ICH guidelines, GCPs and local regulatory requirements.
�Familiarity with FDA requirements.
�Experience in CNS or Oncology therapeutic areas is very advantageous.
SKILLS & PERSONAL ATTRIBUTES:
�Fluency in English is essential
�Independent judgment, tactful discretion, and strong insight.
�Ability to handle multiple tasks to meet deadlines in a dynamic environment essential.
�Strong organisational, presentation, documentation and interpersonal skills as well as a team-oriented approach.
�Basic computer skills in Word, Excel and Email.
�A willingness to travel and be available to attend client and other meetings in Europe.
�Must have valid, current driver's license
BENEFITS OF THE ROLE: If you are looking for excellent working conditions, career development opportunities and a rewarding environment, you will be provided with all of these plus a competitive salary and comprehensive benefits which may include, subject to eligibility and regional variations, pension contribution, life assurance, permanent health insurance and private health insurance plans and childcare vouchers if applicable.
Fforde is a uniquely specialised recruitment agency/business for the pharmaceutical, clinical research and biotechnology sectors.
KEY WORDS: Clinical Research Associate, CRA, Senior Clinical Research Associate, SCRA, Clinical Team Leader, CTL, Clinical Research, Clinical Trials, Clinical Monitoring, Site Management, Clinical Studies, Life Sciences
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