CROMSOURCE

Freelance Clinical Research Associate, Germany - L

Company
CROMSOURCE
Location
Germany
Salary
Competitive
Posted
30 Apr 2021
Closes
30 May 2021
Ref
HQ00002531
Discipline
Clinical Research
Hours
Full Time
Contract Type
Contract
Experience Level
Experienced (non-manager)
Description:
TalentSource Life Sciences is currently searching for an experienced Clinical Research Associate (CRA) to join one of our partner companies, a pharmaceutical company involved in a wide range of therapeutic areas in Germany.

As a CRA you are of course passionate about clinical trials. You manage your work independently, but at the same time you work in collaboration with trial team members on one of the clinical trials.

Position Duties & Responsibilities:
  • Visit study sites for monitoring visits
  • Review of investigator site files, source records and quality checks
  • Possibly also for remote monitoring of the eCRF
  • Roughly 20-30 sites running in Germany during 2021
  • Plan additional sites in the coming years, no end-date has yet been defined
  • Coordinating with cross discipline team members to make sure that all parties are on track with project requirements, deadlines, and schedules
  • Submitting project deliverables and ensuring that they adhere to quality standards
  • Input clinical research data into electronic data systems
  • Monitor study sites and activities to ensure the appropriate industry protocols and terms of the study are being followed
  • Create thorough documentation of study protocol and update it as needed


Education, Experience and Skills:
  • Preferably life sciences degree with experience in a clinical research/healthcare environment or qualified nurse/healthcare professional
  • Ideally at least 2-3 years of experience as CRA
  • Detailed knowledge of required procedures for monitoring clinical trials and of GCP; and local regulatory requirements
  • Knowledge of the local and international law relating to the conduct of clinical research
  • Current/Valid ICH-GCP training
  • Familiar with medical terminology
  • International and intercultural work experience is beneficial
  • Advanced English and local language skills (spoken and written) any other European language is an asset
  • Excellent verbal and written communication skills
  • Well-developed communication skills
  • Ability to work in an international team
  • Organisational skills
  • Knowledge of project management principles
  • IT skills (word, excel, power point)
  • Accuracy & attention to detail
  • Collaboration & teamwork
  • Pro-active and Flexible


Who will you be working for?

About CROMSOURCE

CROMSOURCE is a family owned international, full-service Contract Research Organisation who, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. The successful growth of CROMSOURCE has been achieved by putting high quality and client focus at the heart of everything we do.

Our Company Ethos

Our employees are the most valuable company asset. We value our resources and ensure they work in a friendly, family environment so they are able to develop their skills and talents. Human Resources is the fulcrum around which all CROMSOURCE activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives to all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values are evidenced by our below industry average turnover rates.

About TalentSource Life Sciences

TalentSource is the division of CROMSOURCE dedicated to flexible staffing solutions. Through us, you will have the opportunity to be integrated into a sponsor-led team, whilst having the continuous support from your Line Manager, who will work closely with you to mentor and support your professional development and growth. For our client-facing positions, you must be confident, be able to drive the role and work autonomously.

The Application Process

Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.

If you would like to discuss the role before applying through the website @ https://www.talentsourcelifesciences.com/job-information/?job-id=HQ00002531

or please contact Rocio.EgeaMota@cromsource.com for more information.

CROMSOURCE is an equal opportunities employer. All qualified applicants will receive consideration for employment in relation to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran or military status or any other legally protected status. CROMSOURCE is also committed to compliance with all fair employment practices regarding citizenship and immigration status.

Keywords: Clinical Research Associate, Freelance, Freelancer, Monitoring, GCP
Skills: Clinical Research Associate, Freelance, Clinical Research Organisation, CRO, GCP, ICH-GCP, Monitoring, Regulatory, remote monitoring Location: Germany Share:

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