Key responsibilities: Lead and coordinate pre-formulation, formulation and process development tasks and represent pharmaceutical development in the project team Accountable for managing all pharmaceutical development
Key responsibilities: Lead and coordinate pre-formulation, formulation and process development tasks and represent pharmaceutical development in the project team Accountable for managing all pharmaceutical development
Clinical Development Quality Lead
Key responsibilities: 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
Global Project Leader Oncology
Key responsibilities: Guide innovation, provide drug development expertise and strategic leadership to the Programs and project teams, comprising all pre-clinical, clinical, technical, regulatory, operational and
Recruitment Manager Digital Healthcare
Key responsibilities: Following clearly defined briefs from our clients, your focus is to drive diligent filtering of applications, reviewing CVs, vetting candidates, interviewing and evaluating
Leads and facilitates cross-functional interfaces and interactions within the Clinical Trial Team and external partners (i.e., CRO and other vendors)
Program Operational Lead, Clinical Operations
Serves as a core member of Core Team and Sub-team(s) representing Global Clinical Operations and contributes to the development of the Clinical Development Plan of the assigned program/indication
Lead the development and implementation of the site R&D strategy including alignment with the site objectives and Global R&D.
Responsibility for leading the development, scale-up, registration/validation of drug substance, particle engineering and drug development programs for the site.
Key responsibilities: Audit & CAPA process owner On behalf of the Head of Quality, act as business owner for “Audit & CAPA System”: single point
Consultant Clinical Scientist Oncology (6-months full time role)
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)
Senior Clinical Development Director Oncology ( Early Development)
Provides the strategic direction and clinical development plans (definition and updates). Is a permanent member of Core team, leader of the clinical sub-team and depending on the program, may also be a member of study team…
The Execruit team brings an unparalleled expertise and passion to address your talent recruitment, leadership assessment and development, career development, outplacement and e-learning requirements.