You assist the Director in managing the Clinical Trials Specialist Group, focusing on standardizing practices, training team members, and ensuring regulatory compliance while tackling project challenges.
Anforderungen
- •Bachelor's degree in life sciences
- •Advanced degree preferred
- •10 years in pharmaceutical/biotech industry
- •5 years in Global Clinical Development Operations
- •Line management experience in pharma/CRO/biotech
- •Experience with inspection readiness and audits
- •Strategic thinking and leadership abilities
- •Proficiency in electronic data systems
- •Strong communication and presentation skills
- •Advanced skills in Microsoft Office
- •Ability to manage change
- •Excellent networking and stakeholder management skills
- •Detail-oriented with strong critical thinking
Deine Aufgaben
- •Support the Director in leading the CTS group.
- •Develop and implement work practices for the CTS group.
- •Assist with resource allocation and team onboarding.
- •Provide training on processes and best practices.
- •Ensure compliance with regulations and procedures.
- •Serve as a point of escalation for project challenges.
Deine Vorteile
Wellbeing support for team members
Competitive remuneration packages
Original Beschreibung
# Associate Director Clinical Trials Specialist Group
London, United Kingdom; Mainz, Germany | full time | Job ID: 9113
The Associate Director Clinical Trial Specialist Group, supports the Director (CTS Group Leader) in providing leadership and strategic management of the CTS group. This role ensures the standardization of administrative tasks in support of Clinical Trial Managers within Clinical Operations, contributing to the consistent, high-quality execution of clinical trials.
**Your Main Responsibilities Are**
* Support the Director in leading the CTS group and ensuring standardization of administrative tasks
* Develop and implement work practices and standards for the CTS group
* Assist in resource allocation and onboarding of new team members
* Provide training and updates to the CTS group on processes and best practices
* Ensure compliance with regulatory requirements and company procedures
* Serve as a point of escalation for project challenges and negotiate resolutions
**What You Have To Offer**
* Bachelor’s degree in life sciences or a related field; advanced degree preferred
* Minimum of 10 years of experience in the pharmaceutical/biotech industry, with at least 5 years in Global Clinical Development Operations
* Previous line management experience in pharma/CRO/biotech
* Experience with inspection readiness and audit preparations
* Strategic thinking and leadership abilities
* Proficiency in electronic data systems (e.g., eTMF, IRT, EDC, CTMS)
* Strong communication and presentation skills
* Advanced skills in Microsoft Office programs
* Ability to manage change and guide the CTS group through adjustments
* Excellent networking and stakeholder management skills
* Detail-oriented with strong critical thinking and decision-making abilities
**Your Benefits:**
BioNTech is committed to the wellbeing of our team members and offers a variety of benefits in support of our diverse employee base. We offer competitive remuneration packages which is determined by the specific role, location of employment and also the selected candidate’s qualifications and experience.
Note: The availability, eligibility and design of the listed benefits may vary depending on the location. The final requirements for the individual use of our benefits are based on the company's internal policies and applicable law.
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