Pre-clinical Study Manager

Location Warszawa
Offer description

We are an international Executive Search boutique company focused on providing our Clients with the best HR solutions. We have been recruiting for the top and key positions in Life Science and Medical Technology companies for many years.

At present, we are proud to be working with a Polish innovative biotechnology company.  Together with our Client, we are looking for an established, senior professional, for the position of Pre-clinical Study Manager, who will manage research activities in preclinical stage for development in and oncology diseases.

Duties Key Tasks:
• Generate, lead and support detailed research plans to drive the progress of two preclinical programs in autoimmune disease through IND filing to clinical development readiness.
• Collaborate with the lead scientists on the in vitro, ex vivo and in vivo experiments to address knowledge gaps relative to pathway biology, biomarkers and disease indications across all programs.
• Collaborate with lead scientists on the set-up and maintenance of key research collaborations [such as contracts, materials transfer, timelines financials] with leading academic investigators and CROs in the areas of respiratory, inflammation, oncology relevant to disease pathogenesis and pathway biology.
• Apply scientific know-how and project management experience to direct collaborative relationships with internal stakeholders, external contractors and with the company research leadership to resource and advance projects, develop reports and metrics for communicating program status to inform all levels in the organization.
Required skills Requirements:
• BSc or MSc with minimum 5 years’ experience in managing research projects in the life sciences industry ( degree would be a plus).
• Strong scientific background with solid experience in project execution and operational management of research and preclinical programs through IND phases.
• Demonstrated experience in conducting drug safety assessment studies, management of multiple scientific projects, and solid track record of sound scientific interpretations and risk assessments required with understanding of the overall drug development process.
• Expertise in the following therapeutic fields: oncology, respiratory diseases, fibrotic diseases.
• Experience in biomarker development is preferred.
• Experience working with internal IP, business development, toxicology clinical development stakeholders is highly desirable.
• Experience working with multi-disciplinary and matrixed teams.
• Excellent team building, leadership and management skills.
• Excellent listening, communication and interpersonal skills fostering team spirit.

The Offer:

• Contract of employment;

• Base salary, with stock options and performance-related bonuses;

• Necessary working tools – laptop, mobile phone etc.;

• Benefits such as private healthcare etc.;

• Occasional business travels.

Last modified Monday, October 29, 2018