CRA

Employer
Docs Global (Continental Europe)
Location
Netherlands
Salary
Competitive
Closing date
10 Oct 2020

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Discipline
Clinical Research, Clinical Research Associate
Hours
Full Time
Contract Type
Permanent
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• Recognise, exemplify and adhere to ICON/DOC's values which center around our commitment to People, Clients and Performance.
• As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes addition value to our business and meeting client needs.
• Work according to and comply with relevant ICON/DOCS procedures and processes as applicable.
• Work according to an comply with Sponsor processes and systems as applicable.
• Ensure accuracy and completeness of data enterd into Sponsor systems as applicable.
• Independent and proactive coordination of all the necessary activities required to pre-qualify,initiate, monitor and manage, close-out a study including the following:
• Knowledge of ICH-CGP and Clinical trial processes and operations plus local codes of practice as applicable

Experience
• Experience should include monitoring skills. Experience should be a minimum of 2 years of active independent on-site and field monitoring and site monitoring experience.

Competencies
• Ability to learn and acquire detailed knowledge of disease under study, protocol, investigational product, regulatory requirement in a limited period of time and work in different teams, with different protocols, systems, platforms and apply prior learnings to current situation.
• Ability to review and evaluate clinical data.
• Ability to work pro-actively, in a collaborative way,solve problems, prioritize and assist others to meet study timelines and deliverables.
• Ability to work independently.
• Ability to work in regulated environment, comply with quality, service and productivity standards.
• Fluent in local language(s) and English; written and oral.
• Good oral and written communication skills.
• Computer literacy including but not limited to Clinical Trial Management System, Electronic data capture systems and MS-Office products.
• Due to the nature of this position it may be required for the employee to travel. Therefore, dependent on the employee's location, the employee may be required to possess a valid Drivers license.
Education
• Degree in life sciences, medicine, nursing or related field

#CRAjob

DOCS provides global strategic resourcing and FSP services to the biopharmaceutical and medical device industries. Founded in 1997, DOCS has grown to become the premier resourcing provider for the clinical development industry. 

 

Our Values

At DOCS, we are driven by our core values that guide our culture and support our goal to become a Trusted Partner. Our five core values are:

OUR PEOPLE: We attract, source, develop and retain the best talent to enables us provide world-class people and solutions for our clients.

EXCELLENCE: We never stop looking for new, better ways of working.

ACCOUNTABILITY: We take responsibility for our actions, owning our client’s problems and proactively looking for solutions.

INTEGRITY: Becoming a trusted partner means being honest, respectful and ethically sound, at all times.

OPENNESS: We encourage and facilitate an open and inclusive environment for a diverse global network of employees and stakeholders.

Contact Us
  • 2 Globeside
  • Globeside Business Park
  • SL7 1HZ
  • United Kingdom
  • +44 (0) 2380 688500
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