INSIGHTS

Global Licensing Director

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

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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.

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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)…

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Senior Global Program Manager

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.

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Global Program Head

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

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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)

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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

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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.

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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

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The Execruit team brings an unparalleled professional dedication to address your talent recruitment, leadership development & assessment, career development, outplacement and e-learning requirements.

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