Seattle Genetics Jobs in Berwyn

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The Graphics Specialist will prepare publication graphics and design scientific poster layouts. The position also acts as a technical expert in document templates and formatting. RESPONSIBILITIES: · Develop graphics for content with a technical/scientific orientation, e.g., developing biotech, medical, or life-science figures and images · Lay out scientific posters with content developed by sci...

We are currently seeking a Medical Writer to write and revise clinical documents for submission to the FDA and other regulatory agencies, and to support other clinical communication efforts including abstracts and presentations for medical congress meetings and manuscripts for peer-reviewed journals. RESPONSIBILITIES: · Write and edit clinical study reports, study protocols, investigator’s broch...

Research Associate III – Job Description Major Duties and Responsibilities: · Develop and assist in development and qualification/validation of ligand bind assays and electrochemiluminescence (ECL) assays. · Preparation of Bioanalytical reports and Validation reports. · Routine performance of ligand binding assays in the testing of clinical and non-clinical samples under GLP (Good Laboratory P...

Receptionist Seattle Genetics is looking for an enthusiastic, professional individual to join the team as the front desk receptionist. This position is responsible for front office reception and administration duties, including greeting guests, answering phones and company inquiries. This position reports into Human Resources and offers an opportunity to learn more about the Human Resources funct...

Safety Physician, Safety Evaluation & Risk Management (SERM) The Medical Director SERM will be responsible for signal detection and aggregate safety assessment for global pharmacovigilance and risk management for assigned Seattle Genetics, Inc. investigational and/or marketed products. This individual will serve as a member of the Drug Safety department and function in a company matrix team envi...

This position reports to Medical Director – Clinical Development and will contribute in the clinical arena of hematologic malignancies. The successful candidate will function as a scientific and medical resource for the Clinical Affairs department at Seattle Genetics, and as a medical monitor for ongoing clinical trials in oncology. Responsibilities: · Development of clinical protocols and amend...

Major Duties and Responsibilities: Research Associate (RA) will work in a collaborative setting with other cell line and cell culture development staff on CMC development projects. RA’s primary responsibility is to support recombinant cell line and cell culture development. This will include recombinant protein productions, maintaining clinical and research cell lines, solution and cell culture m...

Major Duties and Responsibilities Requirements (technical skills, key characteristics, education) · As primary submissions manager you will manage the flow of CMC regulatory submissions/technical content from a diverse range of development experts · Develop/refine department instructions such as: formatting checklist, editing checklist, IND process, data verification · Review, edit and facilit...

Responsibilities: Oversight and review of marketing / promotional and sales training materials Verify medical accuracy, fair balance, completeness of materials and accuracy of citations Determine whether data conveys accurate and non-misleading messages or impressions of the product Interface and collaborate with Commercial Project Sponsors of materials to resolve issues and questions about ma...

JOB SUMMARY: This position focuses on coordination of all clinical operations site management and monitoring activities required to initiate, monitor and complete clinical programs at the clinical trial site level. May act as mentor for less senior members of the Clinical Trial Team. Provide the clinical operation input to the clinical project team. DETAILEDDUTIES & RESPONSIBILITIES TYPICALLY IN...

JOB SUMMARY: This position is responsible for supporting the Quality department by ensuring that systems are operational and GMP compliant where required. Management activities of systems may include administrative tasks, maintaining system security, end user training and issue identification and trouble shooting. The core function consists of day to day Electronic Data Management System (EDMS) t...

Position Summary: The Manager, Market Planning actively participates in Seattle Genetics’ commercial planning efforts by providing unbiased, objective, in-depth information about current and future markets, product performance, customers, and competitors. He/she connects and analyzes multiple data sets to identify trends and develop insights that inform commercial strategy. Major Responsibilitie...

Essential Functions (Responsibilities): The primary responsibility of the Director of Technical Operations is to provide for a stable, secure, documented, scalable and responsive systems environment. The Director of Technical Operations will report to the Vice President, Information Technology and will work closely with other IT leadership, customers and vendors (inc. data center and network prov...

Medical Director/ Sr. Medical Director, Safety Evaluation & Risk Management (SERM) The Medical Director/ Sr. Medical Director SERM will be responsible for strategic medical leadership for global pharmacovigilance and risk management activities for assigned Seattle Genetics, Inc. investigational and marketed products. This individual will serve as a member of the Drug Safety leadership team and f...

The Position Seattle Genetics is undergoing significant growth as our oncology pipeline continues to mature. The Human Resources team has an immediate need for an experienced Human Resources professional with strong HRBP and Recruiting expertise to work on a contract basis for a period of 4-6 months. This individual will be expected to help support our HRBP team during a period of particularly he...

The Formulation Group at Seattle Genetics is seeking a Research Associate to participate in the development of lyophilized and liquid formulations for our antibody and antibody drug conjugate programs. Responsibilities: Conduct experiments and analyze results leading to the development of robust formulations for antibody and antibody drug conjugate (ADC) drug substances and drug products Execut...

The successful candidate will be responsible for providing analytical support for the chemical development of novel small molecule anti-cancer drugs and drug linkers used for antibody conjugation. The ideal candidate should possess knowledge of modern chromatographic and spectrometric techniques with demonstrated application of these skills in supporting small molecule process development and prob...

The conjugation process development (CPD) group is seeking an energetic and productive research associate to participate in the development of antibody-drug conjugate (ADC) GMP manufacturing processes. CPD is a close collaborative group that works together to ensure that all group goals are met, but Research Associates in the group act as independent CPD representatives on multi-functional teams, ...

The Accountant will be responsible for assisting with the financial activities supporting the commercial processes. This position will also perform other duties in the area of accounting operations. Major Duties and Responsibilities: Operational support of commercial operations Analysis, review and approval of submitted Medicaid claims invoices Analysis and review of submitted chargebacks Ana...

Responsibilities: · Ability to Execute a Plan of Action (POA) marketing strategies, which includes delivering approved branded sales messages, executing planned programs, scheduling and following-up with medical educational programs, and achieving or exceeding sales targets. · Responsible for servicing and managing accounts, which includes ensuring product access, resolving/triage reimbursement ...