Mainz, Germany; London, United Kingdom | full time | Job ID: 9860
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
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.
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.