Celgene Principal Scientist, Biotherapeutic Bioanalysis in Summit, New Jersey

Description

Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, ​quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries, and growing - we look for talented people to grow our business, advance our science and contribute to our unique culture.

BASIC RESPONSIBILITIES:Principal Scientist (Biotherapeutic Bioanalysis) is a functional leader responsible for managing scientific and technical activities related to preclinical pharmacokinetics, nonclinical/clinical pharmacokinetic bioanalysis and immunogenicity assessments.

SPECIFIC DUTIES:• Responsible for the oversight of development of robust immunoassays for pharmacokinetic and immunogenicity assessments for the assigned discovery and development biotherapeutic programs.• Represent DMPK on cross-disciplinary discovery and development project teams for biologics and cellular therapies, formulating and executing project strategies in collaboration with functional teams.• Provide oversight of CROs for bioanalytical method development, validation and sample analysis for regulated toxicokinetic and clinical studies, and ensure compliance with applicable global standards• Write and critically review BA, Immunogenicity and PK/TK reports, and relevant sections of regulatory dossier in support of IND through NDA submissions.• Represent DMPK in interactions with internal and external stakeholders, as needed.

The position requires an individual with:• An advanced graduate degree in a relevant field (Ph.D., or equivalent) with deep expertise in immunoassay development• Expertise in flow cytometry and qPCR is a plus• Good awareness of regulatory and standard industrial practices in biotherapeutic bioanalysis• Broad understanding of the drug development process• Mentoring skills• Good communication and interpersonal skills to effectively represent function at internal working groups/project teams

Domestic and international travel is mandatory as required.

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Celgene is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Celgene complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must have authorization to work for Celgene in the U.S.COMMITTED TO IMPROVING THE LIVES OF PATIENTS WORLDWIDE

At Celgene, we seek to deliver truly innovative and life-changing drugs for our patients. Our vision as a company is to build a major global biopharmaceutical corporation while focusing on the discovery, the development, and the commercialization of products for the treatment of cancer and other severe, immune, inflammatory conditions.

“At Celgene, we seek to deliver truly innovative and life-changing drugs for our patients.”

There are more than 300 clinical trials at major medical centers using compounds from Celgene. Investigational compounds are being studied for patients with incurable hematological and solid tumor cancers, including multiple myeloma, myelodysplastic syndromes, chronic lymphocytic leukemia (CLL), non-Hodgkin’s lymphoma (NHL), triple-negative breast cancer and pancreatic cancer. As committed as we are to clinical accomplishment, we are equally committed to patient support, which is a guiding principle at Celgene. We believe all who can benefit from our discoveries should have the opportunity to do so. Celgene puts patients first with industry-leading programs that provide information, support and access to our innovative therapies.