SPECIALISTS FOR PROJECTS
IN LIFE SCIENCES
Are you looking for a specialist in the fields of pharmaceuticals, biotechnology or medical technology
to fill a vacant project role?
Within the field of Life Sciences, we provide freelance specialists for the areas of Pharma, Biotechnology and Medical Technology.
Swift and efficient help with projects
We focus on delivering an integrated and holistic service to both our existing and new customers while covering the entire range of job roles available within Life Sciences. One of the unique features of our contracting business is the speed in which we are able to fill vacant positions. We are almost always able to achieve our goal of providing one to a maximum of three highly-qualified and specialised job candidates within 24 to 48 hours.
Being able to provide our customers with freelance specialists gives an extra added value to our service – particularly for individual projects, knowledge transfer or when our customers need extra support to bridge peak workloads or resource bottlenecks.
We can provide you with specialists in the following areas for pharmaceuticals and biotechnology:
- Research and Development
- Clinical Research
- Biostatistics and SAS Programming
- Drug safety, Pharmacovigilance
- Medical Affairs
- Regulatory Affairs
- Medical Marketing
- Sales and Business Development
- Health Economics
- Manufacturing / Production
- Quality management
Research and Development
- Research Technician / Scientist, Project Manager
- Toxicologist, Pharmacologist
- Consultant for Pharmaceutical Development, Galenics
- Consultant for Analytical Development
- Scientist
Clinical Research
- CRA, Senior CRA, Lead CRA
- Clinical Project Manager
- Clinical Study Manager
- Clinical Trail Manager
- Medical Writer
- Line Manager
Biostatistics, SAS Programming, Data Management
- Biostatistician
- Bioinformatician
- Clinical Programmer (SAS, Oracle)
- Statistician
- Clinical Data Manager
Drug Safety, Pharmacovigilance
- Drug Safety Officer, Manager
- Pharmacovigilance Officer, Manager
- Risk Management Specialist
- Safety Writer, QPPV
Medical Affairs
- Medical Affairs Manager
- Medical Liaison Manager
- Medical Writer
- Medical Scientific Manager
- KOL Management
Regulatory Affairs
- Regulatory Manager
- Regulatory Dossier Writer (Module 1-5)
- Regulatory / Technical Writer
Medical Marketing
- Product Manager
- Brand Manager
- Medical Marketing Manager
- Medical Writer
Sales and Business Development
- Manager Business Development
- Manager for Portfolio Optimization (in-licensing / out-licensing)
Health Economics
- Manager for Outcomes Research, HEOR
- Manager Market Access
- Manager for Pricing and Reimbursement
Manufacturing / Production
- Head of Production / Production Manager, Team Leader, Production Management
- Supply Chain Management
Quality Management
- Manager Quality Control
- Manager Quality Assurance
- Qualifier, Validator, IT validations pharma according to ICH, ISO, GMP and FDA
- Qualified Person according to §14 AMG and to §15 AMG
- Auditors (GLP, GCP, GMP, GSP, GDP), FDA Mock-Audit
- Supplier audit
- CAPA Management
We can provide you with experts in the following areas of medical devices:
- Regulatory Affairs 1-III
- Risk Management
- Certification procedures according to conformity assessment
- Complaint Handling
- Computer System Validation (CSV)
- Medical Devices Software
- Life Cycle Management
- Medical Devices Safety
- Diagnostics, in-vitro / in vivo
- Market Access
- International Project Management
- Audit Management
- Business Development
- Research and Development
- Clinical Research, Evaluation and Monitoring
- Clinical Research Associate
- Medical Marketing
- Medical Writer
- Produkt Management
- Project Management
- Quality Management
The list only represents a small portion of our portfolio. It is dynamic and subject to change as rare skills are a hallmark of our service offerings.