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of Position The Manager/Senior Manager, Cell Culture Manufacturing is responsible for planning and driving the execution of manufacturing activities in the Cell Culture area of a cGMP manufacturing area. This position will forecast monthly and weekly activities, plan daily activities and ensure staff are focused on these activities. He/She will motivate the team and drive
Posted 3 days ago
of Position The Senior In House CRA will act as a key agent for the operational set up, delivery and close out of clinical trials day to day management of vendor interaction, and the development of study documents and plans. She/he will participate in the planning, implementation and general oversight of clinical trial activities in conjunction with the project leader. Wil
Posted 5 days ago
of Position The Associate Clinical Research Director/Clinical Research Director provides medical input to all aspects of product development, for new and innovative treatments being developed in patients. Will serve as scientific and medical member for clinical team(s) working closely with clinical project lead, the regulatory Lead, and the operational lead(s) for overall
Posted 6 days ago
The Associate Clinical Scientist/Clinical Scientist is responsible for providing input into the global clinical development plans and strategy, while supporting both clinical trial conduct and safety surveillance activities that contribute to efficacy analysis and risk management planning for products under development. He/she supports assigned clinical development physic
Posted 6 days ago
of Position The Clinical Database Developer II/III is responsible for the design, development, implementation, modification, and support of one or multiple clinical trial databases in support of MacroGenics clinical trials. This entails designing and developing electronic Case Report Forms (eCRFs), related edit checks, other database objects and documentation to meet proje
Posted 6 days ago
of Position The responsibilities of this position include performing and overseeing Quality Assurance (QA) activities that support reference standard and cell bank release process for clinical and commercial batches and support Quality Control method validation and stability testing. The incumbent in this role will review, evaluate, and approve all GMP data supporting Cell
Posted 6 days ago
of Position This individual will provide in vitro and in vivo pharmacology expertise to support the Company's antibody based oncology product candidates including both pre clinical and clinical stage programs, reporting key program milestones and timelines to project teams. Responsibilities Proposes and validates novel immune oncology (IO) based therapeutic strategies leve
Posted 6 days ago
of Position The responsibilities of this position include performing quality assurance activities that support Good Manufacturing Practices (GMP) related to clinical/commercial lot release. He/she will interface with other departments and will provide guidance, make recommendations and in some cases, resolve a variety of GMP and other quality issues that arise. Responsibil
Posted 7 days ago
of Position The responsibilities of this position include performing and overseeing quality assurance activities that support all QA aspects of the drug substance release process for clinical and commercial batches. The incumbent in this role will review, evaluate and approve all GMP data supporting lot release. As the lead, the incumbent will oversee the review and releas
Posted 7 days ago
of Position The Development Associate I/II position will be responsible for supporting drug substance and drug product formulation development for biologics molecules from early to commercialization stage. This is a hands on position in the laboratory involving design and execution of experiments to develop stable biologics formulation and monitoring stability by utilizing
Posted 7 days ago
of Position The Sr. Clinical Sites Contracts Manager is responsible for managing all aspects of clinical site contracting, negotiation and execution of required agreements in support of the clinical development plan. Responsibilities and Job Duties Develops clinical study specific negotiation parameters, both for budgets and legal language to ensure consistency and standar
Posted 7 days ago
of Position The Scientist I is responsible for analyzing antibody repertoires from immunized animals by next generation sequencing, identifying lead panels of antibodies for biotherapeutic development, and further developing our multi specific antibody formats. He/she will play a key role in advancing our antibody discovery platform and driving new therapeutic projects fro
Posted 10 days ago
of Position The Sr. Human Resources Business Partner (HRBP) is responsible for driving and/or executing HR strategies, managing the day to day aspects of a client group, and championing initiatives that positively impact organizational effectiveness including employee engagement and culture, team building, and people development. She/he will achieve this by working closely
Posted 10 days ago
of Position The Data Manager II/III collaborates with various departments on the design, documentation, testing and implementation of clinical data studies. Develops systems for organizing data to analyze, identify and report trends. Analyzes the interrelationships of data and defines logical aspects of data sets. Prepares reports of clinical trial studies for internal val
Posted 11 days ago
of Position The Development Scientist I/II is responsible for the development of Drug Product (DP) formulation and manufacturing processes for the Company's pipeline molecules across early and late stage clinical and commercial development. Represents the Drug Product Sciences (DPS) group in cross functional project teams and leads DP development activities within DPS, inc
Posted 11 days ago
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