Clinical Research Associate - Remote, Germany

Company
Synteract
Location
Germany
Salary
Competitive
Posted
25 Feb 2021
Closes
27 Mar 2021
Ref
28775
Discipline
Clinical Research
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)
Clinical Research Associate (CRAII or SCRA) - Anywhere, Germany
Office-based or Remote-based

Who We Are

Synteract ® , a Syneos Health ® company, is a leading full service Contract Research Organization (CRO) with a successful three-decade track record of supporting emerging biotech and pharmaceutical companies. We provide customized Phase I through IV services globally, offering expertise across multiple therapeutic areas, including notable depth in oncology, dermatology, general medicine, infectious disease and vaccine, neuroscience, pediatrics, and rare and orphan diseases.

Position Overview
The Clinical Research Associate II / Senior Clinical Research Associate is responsible for the monitoring of clinical trials and tracking of study progress, thereby contributing to the overall management of clinical trials in accordance with the appropriate quality standards including ICH-GCP guidelines, Standard Operating Procedures (SOPs), applicable regulations, rules and guidance. S/he is responsible for clinical site start-up, maintenance, and closure activities, including maintenance of study documents. *Note, the Clinical Research Associate II / Senior Clinical Research Associate level will be determined based upon individual experience.

Specific tasks would include:
  • Responsible for the monitoring of clinical trials throughout Poland and tracking study progress for our clients
  • Interface with the Synteract study team to ensure timely initiation and completion of clinical trials
  • Collect study related data and assist with the preparation, review and submission of regulatory documents to regulatory authorities
  • Contribute to the overall management of trials in accordance with ICH-GCP standards, local requirements and SOPs
  • Start-up, maintenance and closure activities of clinical studies including the maintenance of the TMF and study documentation

Qualifications:
  • Degree in life science
  • 2+ years experience as a CRA
  • Good scientific knowledge and understanding of clinical trials
  • Good ICH-GCP knowledge and legal regulatory requirements
  • Motivated, dedicated and service orientated approach
  • Distinctive organizational skills, good time management and ability to meet deadlines
  • Very good English skills (verbal and written), plus local language, IT proficiency
  • Willingness to travel

If you're passionate about clinical trials, we encourage you to apply today!

Synteract's policy is to provide equal employment opportunity and affirmative action in all of its employment practices without regard to race, color, religion, sex, national origin, ancestry, marital status, protected veteran status, age, individuals with disabilities, sexual orientation or gender identity or expression or any other legally protected category. Candidates must possess current and valid authorization to work in the country to which they are applying.

#LI-DL1 #LI-REMOTE

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