Project Management Associate - Mannheim, Deutschland - SCOPE International
vor 2 Wochen
Beschreibung
The organization of international clinical trials requires the development of complex cross-cultural teams across borders, languages and time-zones.At SCOPE International we recognize that recruitment, training and retention of talented employees is fundamental to building high performing teams.
Our success is built upon encouraging talented people to join SCOPE and further training them continuously and systematically to develop their skills and achieve their full potential. We actively seek out recruits who exhibit our key values of customer orientation, entrepreneurial thinking, conscientiousness and reliability.
As a socially responsible company, we offer an
attractive working environment with an open and flexible employment philosophy, thereby providing working environments conducive to an international setting, coupled with excellent career development prospects and a management culture that is based on an open dialogue.
SCOPE International is an independent Full-Service Contract Research Organization (CRO) with a network of 16 local offices and business entities throughout Europe and USA.
SCOPE offers a complete range of clinical development and consulting services to the pharmaceutical, biotechnology and medical device industries, and is supported by long established partnerships in other geographies.
Our experience and expertise in managing all major indications in clinical phases I - IV makes us the perfect partner for companies looking to work closely together to develop custom solutions and seeking guidance through all development phases.
- We are looking for a Project Management Associate (PMA) in Mannheim, Germany for an officebased position.
Tasks & Responsibilities
- Support of the Project Management Team in administration, organization and coordination of logistic aspects in international clinical trials according to ICH/GCP guidelines, laws and regulations and Standard Operating Procedures (SOPs)
- Support of the Project Management Team in supervision of project specific procedures
- Assistance with setup and maintenance of study specific documentation (trial master file) and tracking tools
- Quality control of project specific documentation
- Organization of internal and external meetings
Qualifications & Requirements
- Life science degree
- Basic knowledge of GCP/ICH rules and relevant laws and regulations
- Personal initiative and high commitment
- Excellent organization and communication skills
- Fluent in English and German
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