Associate Director Clinical Trials - Remote job in Mainz, Germany

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First Name*

Last Name*

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Phone Number*

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Are you an employer or a jobseeker?*

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First Name*

Last Name*

Email*

Phone Number*

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Are you an employer or a jobseeker?*

Message

First Name*

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Phone Number*

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Are you an employer or a jobseeker?*

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Job type: Permanent

Discipline: VP/Head of Clinical Operations

Location: Germany

This vacancy has now expired. Please see similar roles below...

Proclinical Staffing are representing a fast growing Biotech in Germany who are looking for a Associate Director, Clinical Trials, to join their team in home-based position. Being a medium sized company with over 3000 employees globally, our client is looking for an established Clinical Operations professional who has a proven track record within the oncology field who can lead operationally, ideally with a Pharma/ Biotech background. This opportunity will suit a professional who thrives in high performing environment which will elevate you in your career.

Your Main Responsibilities Are

Oversee activities related to the management of CRO and sponsors
Oversee the development and review of portfolio documents such like Oversight Plans, Process Developments and SOP development
Point of escalation in case of challenges in platform or vendor-related activities with other departments or external vendors; contributing to the process of selection and decision on participation of vendors, preferred vendors and partnership vendors
Taking care of team developments, identification of high-performance team members and working on team development
(Assurance of) Adherence to the regulatory requirements, the ICH-GCP guidelines and the respective procedures (i.e. policies, SOPs, instructions)

What You Have To Offer

Natural/ life sciences or medical background (university degree or experience in a medical profession such as Nurse or Medical Technical Assistant or Pharmaceutical Technical Assistant), combined with many years of experience in project management, regulatory submissions and global study organizations
Oncology experience is preferred
Profound knowledge and experience in relevant legislation and international guidelines (ICH-GCP) for the performance of clinical research projects
Profound experience with the preparation and processing of national and international projects under consideration of the local laws, international guidelines (ICH GCP) and applicable SOPs
Excellent communication and ability to recognize problems and provide solutions
Able to rapidly enter in action and to work under stressful conditions
Able to motivate and lead a team

What's on offer? A competitive basic salary + 20% bonus + much more. For more information, please apply.

If you are having difficulty in applying or if you have any questions, please contact Auxanne Rameix

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

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