Docs Global (Continental Europe)

Study Start Up CRA (m/w)

Location
Home based anywhere in Germany or office based in Munich, Germany
Salary
Competitive
Posted
20 Jul 2019
Closes
09 Aug 2019
Ref
Ref AS-029810
Discipline
Clinical Research
Hours
Full Time
Contract Type
Contract
Experience Level
Experienced (non-manager)


Job Summary

If you are seeking a career where you can truly make a difference in the lives of others, working closely together with the top minds in Biotechnology, then here is your chance. To strengthen our internal SSU Team, DOCS is hiring a Study Start-up CRA (m/f) to work closely with one of the most successful international biotech companies.

Roles & Responsibilities of the position

• Work independently on EC and local authority submissions in Germany
• Manage document amendments and corrections as requested by the authorities
• Provide input into feasibility, identify clinical investigators and conduct site evaluations post-feasibility to determine site suitability and selection
• Conduct occasional site visits as necessary for SSU purposes
• Responsible for study start-up activities, including creating site folders, collating, preparing and maintaining (e)SIP documents and updating systems in collaboration with the CTA-Team
• Ensure collection, review, track and provision of appropriate clinical documents to support regulatory submission and to perform IRB/IEC submissions including preparation and submission of all documents to the central and/or local committee

Job Requirements

• BSc. or MSc. degree in life sciences or equivalent
• Several years of experience working as CRA and/or as SSU (working on industry-sponsored or industry-partnered clinical trials at academic institutions, or working on clinical trials at a biotech, pharmaceutical or CRO company)
• Strong experience within study start-up, especially in EC trial submissions phases 1,2,3 and NIS and BfS submissions with a track record of having managed submissions independently from start to finish
• Attention to detail, organizational skills, time management & prioritization
• Proficiency in English and German
• Good working knowledge of common software packages

Remuneration & other details

• Home-office with very occasional travel
• Friendly work environment
• Interesting trials in various therapeutic areas
• Possibility to gain solid experience in a global pharmaceutical company
• Unlimited employment contract with DOCS
• Compensatory time-off
• Contribution to pension scheme
• Chance to work with one of the leading companies, that has implemented Risk Based Study Execution (RBSE)
• Chance to work on First-In-Human trials

Would you like to know more? Please submit your CV to timo.kindermann@docsglobal.com or contact us on +49 89 666 105 162. We are looking forward to your application.

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