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- Aufgaben: Lead and manage clinical trials, ensuring compliance with regulations and timelines.
- Arbeitgeber: Join BioNTech, a pioneering biotech company focused on innovative therapies.
- Mitarbeitervorteile: Enjoy competitive pay, diverse employee support, and a collaborative work environment.
- Warum dieser Job: Make an impact in healthcare while working with a passionate team in a dynamic setting.
- Gewünschte Qualifikationen: Degree in life sciences or medicine; 3+ years in project management or clinical trials.
- Andere Informationen: Apply online with your CV and motivation letter to join #TeamBioNTech.
Das voraussichtliche Gehalt liegt zwischen 43200 - 72000 € pro Jahr.
Mainz, Germany; London, United Kingdom | full time | Job ID:8722
The Clinical Trial Manager is responsible for the execution of clinical trials, mainly with regard to operational and administrative aspects. This implies the preparation and processing of national and international projects under consideration of the local laws, international guidelines (ICH GCP) and applicable SOPs. S/he performs activities related with the leading of an operational project team, the supervision/control of third party providers, the timely performance of all services, as well as the problem management by interacting with all departments involved.
Your main responsibilities are:
- Support in preparation of regular status reports to Platform and Portfolio leads, and Chief Medical Officer (CMO), including presentation of project status in meeting
- Overlooking the clinical operation trial budget
- Opportune contact with Project Manager and Platform lead in case of divergences from the project plan
- Oversight on project timelines and deliverables
- Set-up or oversight of study related documents such like Trial Management Plan, Monitor Manual, etc.
- Contribution to and review of study core documents, e.g. synopsis, investigator’s brochure, patient informed consent documents etc.
- Coordination of project activities with other internal departments or external vendors from start-up to close out of a clinical trial
- Instruction and supervision of CTCs, CRAs and CTAs (in the scope of a project)
- Point of contact in case of problems within the clinical trial
- Support in planning and conduct of project training prior to starting project activities, oversight
What you have to offer:
- Background in natural/life sciences or medicine (University degree or experience in a medical profession such as Nurse, Medical Technical Assistant, or Pharmaceutical Technical Assistant)
- Minimum of 3 years of experience in project management, regulatory submissions, monitoring of clinical trials, or clinical trial coordination
- Profound knowledge and experience in relevant legislation and international guidelines (ICH-GCP) for the performance of clinical research projects
- Very good English (written and spoken)
- Experience in usual software (Word, Excel, Power Point, MS Projects)
- Able to recognize problems and provide solutions
- Good organizational and communicative skills
- Pro-active way of working & ready to take over responsibility
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.
How to apply:
Apply now by sending us your application documents including Curriculum Vitae, copy of ID, copies of degree certificates and professional certificates, motivation letter as well as your contact details via our online form.
Please note:
Only applications sent via our online form shall be considered. By submitting your application, you acknowledge that a background check will be conducted as part of the recruitment process in accordance with applicable laws and regulations. If you are considered for the position, BioNTech will conduct the background check through our service provider ‘HireRight’. You will be informed accordingly by your BioNTech-Recruiter.
We are looking forward receiving your application.
Inspired? Become part of #TeamBioNTech.
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Manager Clinical Trial Arbeitgeber: BioNTech IMFS
Kontaktperson:
BioNTech IMFS HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Manager Clinical Trial
✨Tip Number 1
Familiarize yourself with ICH GCP guidelines and local regulations relevant to clinical trials. This knowledge will not only help you in interviews but also demonstrate your commitment to compliance and quality in clinical research.
✨Tip Number 2
Network with professionals in the clinical trial field, especially those who have experience with BioNTech or similar companies. Attend industry conferences or webinars to make connections that could lead to valuable insights and recommendations.
✨Tip Number 3
Prepare to discuss specific examples from your past experiences where you successfully managed clinical trials or resolved issues. Highlight your organizational skills and ability to work proactively, as these are key traits for the role.
✨Tip Number 4
Stay updated on the latest trends and advancements in clinical research. Being knowledgeable about current developments can set you apart during discussions and show your passion for the field.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Manager Clinical Trial
Tipps für deine Bewerbung 🫡
Understand the Role: Make sure you fully understand the responsibilities of a Clinical Trial Manager. Familiarize yourself with the key tasks mentioned in the job description, such as project management, oversight of clinical operations, and compliance with ICH GCP guidelines.
Tailor Your CV: Customize your CV to highlight relevant experience in project management and clinical trials. Emphasize your background in natural/life sciences or medicine, and ensure that your skills align with the requirements listed in the job description.
Craft a Compelling Motivation Letter: Write a motivation letter that clearly explains why you are interested in the position and how your experience makes you a suitable candidate. Mention specific examples from your past work that demonstrate your problem-solving abilities and organizational skills.
Prepare Required Documents: Gather all necessary documents including your Curriculum Vitae, copies of your ID, degree certificates, professional certificates, and contact details. Ensure everything is up-to-date and formatted correctly before submitting your application through the online form.
Wie du dich auf ein Vorstellungsgespräch bei BioNTech IMFS vorbereitest
✨Understand the Clinical Trial Landscape
Make sure you have a solid grasp of the clinical trial process, including ICH GCP guidelines and local regulations. This knowledge will help you answer questions confidently and demonstrate your expertise in managing trials.
✨Showcase Your Project Management Skills
Prepare to discuss your previous project management experiences, especially in clinical settings. Highlight specific examples where you successfully led teams, managed budgets, or resolved conflicts to show your capability in this role.
✨Communicate Clearly and Effectively
Since the role requires coordination with various departments and external vendors, practice articulating your thoughts clearly. Use examples from your past experiences to illustrate how you effectively communicated complex information.
✨Prepare for Problem-Solving Scenarios
Be ready to discuss how you approach problem-solving in clinical trials. Think of specific challenges you've faced and how you overcame them, as this will showcase your proactive attitude and ability to take responsibility.
