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Deputy Director Global Clinical Immunology

Position Title: Deputy Director Global Clinical Immunology

Position Requirements:

The Global Clinical Immunology (GCI) Project Representative manages the interactions between GCI and internal/external customers while

ensuring relevant departmental deliverables are met.? The Project Representative works closely with testing platform leaders in GCI and study directors, program managers, study monitors, and

statisticians in Clinical, Medical Affairs, and SPMSD to ensure timely completion of serological testing needed to support licensure and

registration submissions while taking into account overall project timelines and prioritization mandates.

The GCI Project Representative will also provide clinical immunology expertise to Project and/or Clinical Teams. The GCI Project

Representative may serve as a leader or member of working groups and project sub-teams and contributes to the GCI budgeting, capital

expenditure, and facilities and testing processes.? The position will also interact with KOLs and other external testing laboratories. Lead efforts to develop laboratory testing in external

laboratories, which may involve in technology improvements and transfers.

Basic Qualifications:

Education/Years Experience/Other Skills:

PhD or other doctoral degree in Biological Sciences with at least 3-5 years relevant industry experience.

Focus in infectious disease area, preferably in vaccine related fields with immunology experience and expertise is a plus.

Must know how to professionally move projects along a timetable and process driven map.

Demonstrated experience with project management and expertise in a scientific area such as Bacteriology, Virology, Vaccinology, Immunology, Epidemiology, or Microbiology. Knowledge of relevant immunological and microbiological assay techniques is required.

Knowledge of clinical diagnostic, biomarker discovery, translational medicine/science, functional assays, cell based assays, and multiplex assays is a plus.

An understanding of pharmaceutical/biological product development is expected; as well as an understanding of compliance areas such as GCLP, GCP, GLP, or GMP.

Experience writing and reviewing regulatory documents such as IND, CTDs, clinical trial protocols, CSRs, and eBLA sections.

The successful candidate will possess he following competencies:

Excellent communication skills (both oral and written).

Must demonstrate all applicable competencies and behaviors including strategic thinking, high commitment to customers, ability to cooperate transversally across multiple functions and cultures, to act for change while continually striving for targeted results.

Must be able to demonstrate leadership skills, act as a role model to the team and promote good communication and teamwork within the scientific team.

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

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At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.



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