×
Hier anmelden um sich kostenlos auf Stellen zu bewerben oder Stellenanzeigen aufzugeben. X

Manager Clinical Trials

in 55116, Mainz, Rheinland-Pfalz, Deutschland
Unternehmen: BioNTech IMFS
Vollzeit position
Verfasst am 2026-01-16
Berufliche Spezialisierung:
  • Medizin/Gesundheitswesen
    Klinische Forschung
Gehalts-/Lohnspanne oder Branchenbenchmark: 60000 - 80000 EUR pro Jahr EUR 60000.00 80000.00 YEAR
Stellenbeschreibung

Select how often (in days) to receive an alert:

Mainz, Germany;
London, United Kingdom | full time | Job

The Clinical Trial Manager (CTM) is responsible for supporting the Sr. Global CTM and/or Associate Director Clinical Trials with the execution of a clinical trial(s) or leading the execution of smaller trials, mainly with regard to operational and administrative aspects.

Your main responsibilities are:
  • Support in preparation of regular status reports, including presentation of project status in meeting
  • Overlooking the clinical operation trial budget
  • Opportune contact with Project Manager and Associate Director Clinical Operations 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:
  • 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)
  • Profound knowledge and experience in relevant legislation and international guidelines (ICH-GCP) for the performance of clinical research projects
  • Minimum 3 years of experience in project management, regulatory submissions, monitoring of clinical trials or clinical trial coordination with practice in project planning and structuring

Refined colloquial and correspondence skills (written and spoken)

Very good English (written and spoken)

Experience in usual software (Word, Excel, Power Point, MS Project)

Able to recognize problems and provide Solutions

Good organizational and communicative skills

Pro‑active way of working, used to work Independent and 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.

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.

How to apply:

Apply now by sending us your application documents including Curriculum Vitae, copy of , 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 ‘Hire Right’. You will be informed accordingly by your BioNTech‑Recruiter.

We are looking forward receiving your application.

Inspired? Become part of #TeamBioNTech.

BioNTech, the story

At BioNTech, we are more than just a biotechnology company – we are a community of innovators, scientists, and leaders dedicated to revolutionizing medicine by translating cutting‑edge science into survival. Your contributions here have the potential to improve the health of people worldwide, especially by addressing diseases with high medical needs like cancer and various infectious diseases.

Experience a dynamic workplace that embraces diversity in all its forms. We foster innovation, encourage creativity, and develop business strategies driven by our shared passion for advancing medicine.

Working at BioNTech means striving to achieve medical breakthroughs while growing your career in a meaningful way. Apply today and become part of a mission that has the potential to change lives around the world.

BioNTech does not tolerate discrimination, favoritism or harassment based on gender, political views, religion or belief, nationality, ethnic or social origin, age, sexual orientation, marital status, disability, physical appearance, health status or any other physical or personal characteristics. BioNTech is committed to creating a diverse and inclusive work environment. We are proud to be an equal opportunity employer. The main thing is that you suit us, and we suit you!

#J-18808-Ljbffr
Bitte beachten Sie, dass derzeit keine Bewerbungen aus Ihrem Zuständigkeitsbereich für diese Stelle über diese Jobseite akzeptiert werden. Die Präferenzen der Kandidaten liegen im Ermessen des Arbeitgebers oder des Personalvermittlers und werden ausschließlich von diesen bestimmt.
Um nach Stellen zu suchen, sie anzusehen und sich zu bewerben, die Bewerbungen aus Ihrem Standort oder Land akzeptieren, klicken Sie hier, um eine Suche zu starten:
 
 
 
Suchen Sie hier nach weiteren Stellen:
(nach Beruf, Fähigkeit)
Standort
Increase search radius (miles)

Sprache der Stellenausschreibung
Lebenslauf-Kategorie
Bildungsgrad
Filter
Mindest-Bildungsgrad für die Stelle
Mindest-Berufserfahrung für die Stelle
Veröffentlicht in den letzten:
Gehalt