Company: Docs Global (Continental Europe)
Location: Bad Homburg,Germany
Reference: Ref AS-015321
Closing Date: 30 Mar 17
Salary (£): Competitive
Benefits: Excellent & Comprehensive
Our client is one of the world's leading pharmaceutical companies operating in various therapeutic Areas. For our client’s clinical research division, we are currently hiring a Clinical Development Consultant (m/f) Office Based near Frankfurt Germany.
Roles & Responsibilities of the position
• Study feasibility, site feasibility, site identification (with CRPs) and site selection Clinical studies and Observational Research
• Deliver all regional, local, and corporate portfolio commitments/milestones for sties and trials within responsibility.
• Support local needs of globally outsourced studies within responsibility
• Manage IITs
• Regulatory submissions, in affiliates where this is managed by Clinical Operations
• Manage the allocation of patients within the geography
• Manage Site enrolment performance (Assist in recruitment planning, develop site level risk plan for enrolment, utilize available tools to assess site performance, collaborate with TPO CRA to enhance site performance
• Ensure the site ACDD (Anti-Corruption Due Diligence) process is followed and maintain appropriate Anti-Corruption certification of sites on file
• Primary interface with investigators
• Manage the link between site and the TPO
• Collaborate with partners, Quality, and other study team members to resolve/escalate site specific issues when necessary
• Contribute to and partner with the local medical organization to deliver on department goals
• Manage and develop strategic relationship with current and future investigators
• Potential new sites-prospecting-seeking opportunities to widen future sites with portfolio needs
• Look for opportunities for Portfolio sites, Investigator Networks and Site Management Organizations (CMO)
• Master of Science or equivalent
• Knowledge of or experience of the local Healthcare system/model
• Deep scientific understanding / Therapeutic Area knowledge
• Strong, technical, operational Clinical Operations Expertise
• Willingness to travel to sites (appr. 60%)
• Fluent in English and German
Our client offers an exciting and challenging work environment for clinical research professionals looking for an opportunity to contribute to the success of a company dedicated to researching, developing, manufacturing and marketing pharmaceuticals that improve health and quality of life.
Interested? Please submit your CV to firstname.lastname@example.org. We are looking forward to getting to know you.
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