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Dr. Bernd Eisele
CEO

Dr. Leander Grode
CSO and Director Business Development

Dr. Christiane Meller
Project Manager and Quality Assurance Manager

Dr. Steffi Hansen
Project Manager and Quality Assurance Manager

Dr. Katharina Brett
Clinical Project Manager

Dr. Gerald P. Parzmair
Project Manager

Dr. Fabio Pisano
Project Manager

Dr. Kathrin Schulte
Clinical Project Manager

Dr. Rosalie Ridzewski
Project Manager

Dr. Inci Aydin
Project Manager

Inge Jacobi
Accounting and Controlling

Christoph Schütz
Team Assistant

Career
Open positions
Open position

Project Manager (m/f)
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The goal of Vakzine Projekt Management GmbH (VPM) is to promote innovative ideas and bring projects to life. With this approach VPM has developed into a successful biotechnology company which is internationally recognized.
Currently, VPM offers the opportunity to become part of its team of project managers involved in pharmaceutical development. This means being part of a company of team players and working closely together with experts from all areas of the development chain (research, non-clinical development, manufacture, regulatory, clinical development, patent law, marketing and business development) to successfully move our projects forward to market.
Since 2003, VPM has been active in developing promising biopharmaceutical candidates from academic research to successful clinical proof of concept. Several products, ranging from small molecules, recombinant proteins up to gene-modified live vaccines and other ATMPs, have successfully been brought into clinical phases I and II. Based on this in-depth experience, the VPM team is a reliable partner for tailor- made consultancy and services along the complete pharmaceutical development chain.
Are you looking for new challenges? Do you like structural and analytical thinking and planning? Do you want to take responsibility within a project? VPM is offering you the chance to achieve all of this in an ambitious company.

Job Profile:
- Plan and facilitate clinical development of innovative medicines from bench to clinical proof-of- concept
- Identification of and communication with business and collaboration partners within a designated project and its budget
- Planning and management of
+ Process development and manufacture of medicinal products
+ Pre-clinical studies
+ National and international regulatory interactions
+ Early clinical trial development
+ Budget planning
- Review and evaluation of project proposals
- National and international team work

Requirements:
- Completed doctoral studies in life sciences, medicine or pharmacy
- 2 year experience with pharmaceutical research and development
- Excellent self-organization skills
- Ability to comprehend and oversee complex projects and prioritize required actions
- Enjoy working in cross-functional teams
- Flexibility to travel internationally multiple times per year
- Excellent written and spoken English language skills
- Professional working knowledge of common software packages (Word, PowerPoint, Excel)

Contact details
Vakzine Projekt Management GmbH
Dr. med. Bernd Eisele, CEO
Mellendorfer Str. 9
30625 Hannover
+49 (511) 1699080
info@vakzine-manager.de



Life Scientist as CRA (m/f)
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Since 2003, Vakzine Projekt Management GmbH (VPM) has been active in developing promising biopharmaceutical candidates from academic research to successful business concepts. Several products, ranging from small molecules, recombinant proteins up to gene-modified live vaccines and other ATMPs, have successfully been brought into clinical phases I and II. Subsequently, three out of five development candidates have been out-licensed by VPM. Based on this in-depth experience, the VPM team is a reliable partner for tailor-made consultancy and services along the complete pharmaceutical development chain. Currently, VPM is organizing multicentre clinical trials of Phases I, II and IIb in different Indications in Europe, South Africa and Asia.
In order to strengthen our clinical development team, we are looking for an experienced Clinical Research Associate (m/f). This permanent position is immediately available.

Job Profile:
- Plan and facilitate clinical development of innovative medicines from bench to clinical proof-of-concept
- Support regulatory submission (CTA, Amendments)
- Review, collect and maintain essential documents
- Provide input into feasibility, identify clinical investigators and conducts site evaluations
- Ensures clinical study sites are conducting clinical trials in compliance with the respective protocol, SOPs and applicable ICH/GCP guidelines and regulations
- Ensure appropriate safety reporting as well as tracking and reporting of adverse events
- Identify site needs and site-related issues
- Identify and report non-conformities and develop CAPA
- Assist in preparing sites for audits, review audit reports and contributes to resolve findings
- Build and maintain solid and long-term professional relationships with investigators and site staff
- Ensure timely communication of information between Medical Department and site staff

Requirements
- Master degree in a relevant scientific discipline
- Minimum five years work experience in clinical research and Phase I-III trials
- Profound knowledge of clinical trial processes and operations
- Familiar with ICH/GCP guidelines
- Experience working as a CRA
- Proficiency in English and German
- Good working knowledge of common software packages
- Willingness to frequent national and international business travel
- Organizational skills including time management & prioritization
- Attention to detail
- Problem solver
- Team worker

Contact details
Vakzine Projekt Management GmbH
Dr. med. Bernd Eisele, CEO
Mellendorfer Str. 9
30625 Hannover
+49 (511) 1699080
info@vakzine-manager.de


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