Conduct deal making activities to bring new products in to the company’s pipeline:
Assess strategic business fit and attractiveness of new licensing opportunities
Interact with Search & Evaluation and Market intelligence representatives to build a business case (product attributes, competitive edge, market potential, exit strategy, financial modelling) for new opportunities
Talent Acquisition Manager Life Sciences
Following clearly defined briefs from our clients, your focus is to drive diligent filtering of applications, reviewing CVs, vetting candidates, interviewing and evaluating their experiences and skills – with the ultimate goal of developing strong short-lists of candidates for our clients.
Clinical Development Quality Lead
Develop a “risk-based” compound-specific compliance program contributing to document / data accuracy, ultimately resulting in “dossier acceptability” by respective out-licensing partners (emphasis on eCTD Module 5)…
Work closely with the Global Program Head(s) and Global Project Leaders (GPLs) to support/contribute to the development of the program strategy and its integrated development plan.
Guide innovation, provide drug development expertise and strategic leadership to the programs and project teams, comprising all pre-clinical, clinical, technical, regulatory, operational and commercial disciplines
Senior Clinical Scientist, Clinical Development
Drive development of protocols/protocol amendments for clinical studies. Prepare and/or provide input to clinical study related and other regulatory documents (e.g. CSRs, IBs, PIS/ICFs, SAPs, Data Management Plans, Safety Management Plan, Medical Monitoring Plan, SRC Charter, IND, briefing books)
Associate Medical Director Oncology, Clinical Development
Be an integral member of the clinical development team and the clinical study team and drive execution of the clinical study in partnership with other functions
Translational Medicine G(c)LP Quality Lead
Contribute to Vendor selection and qualification process, assess Vendor’s procedures during selection process, guaranteeing compliance with regulatory requirements & verify G(c)LP certification, for TM vendors contributing to numerous PK & biomarkers assessments in DPI’s pre-clinical and clinical programs
Global Program Lead, Global Regulatory Affairs
Lead, develop and implement the global RA strategy for assigned project. Represent RA in Project Teams and in various other cross-functional teams, such as Clinical Study Teams. Present and defend regulatory plans to Debiopharm internal governance bodies.
Senior Global Clinical Trial Manager Phase 3
Develop clinical strategy for the therapeutic area in the assigned oncology program(s) (oncology – hematology) taking into account current medical practice and unmet needs; advances in both biological sciences and data sources; as well as competitive environment
The Execruit team brings an unparalleled professional dedication to address your talent recruitment, leadership development & assessment, career development, outplacement and e-learning requirements.