- Sun Pharma (Taro Pharma) (Bloomington, MN)
- …managed care accounts, providing the consistent delivery of educational and compliant scientific information in support of Dermatology products. The MSLs will engage ... be trained to respond to complex inquiries in a scientific , fair-balanced, compliant manner serving as a critical field...into Sun and present the research to Sun for review . They will become the point of contact with… more
- Sun Pharma (Taro Pharma) (Billerica, MA)
- Job SummaryThe Sr. Associate Compliance provides scientific support in the root cause analysis and closure of OOS investigations, OOT investigations and product ... System standards, compiles monthly Quality metrics for internal and corporate review , and analyzes trends to implement corrective and preventive actions to… more
- Genmab (Princeton, NJ)
- … review of regulatory documents for regulatory submissions Serve as medical reviewer and expert on promotional and medical review committees Inform ... field of solid tumors, with proven ability to translate and align commercial and scientific goals and objectives into actions. Director will work as an integral part… more
- Genmab (Brooklyn, NY)
- …of World. The role requires scientifically trained individuals with strong clinical/ scientific backgrounds and excellent communication skills able to establish and ... maintain professional relationships with members of the healthcare/ scientific communities in support of Genmab's Haematology and Oncology assets. MSLs conduct … more
- Sun Pharma (Taro Pharma) (Billerica, MA)
- …inspections related to medical device and combination products (FDA/ISO).Management Review meeting ensuring the Quality Management Systems (QMS) is suitable ... with all key vendor/supplier.in all vendor/ supplier change notification review and approvals.Annual supplier/vendor assessment, maintenance of supplier/vendor audit… more
- Genmab (Rocky Hill, NJ)
- …operations across Genmab therapeutic areas and to serve as lead for initial review of all corporate funding requests, ensuring close oversight and coordination of ... of all program support. Lead and manage all Grants for Scientific Advancement (GSA) requests pertaining to fellowships, third-party investigator awards, closed… more
- Sun Pharma (Taro Pharma) (New Brunswick, NJ)
- …identification and implementation of improvements needed through routine CMO business review .Implement and maintain Regional CMO data in the Global CMO ... to Sun Pharma requirements, are regularly reviewed and followed.Conduct review and approve batch release documentation.Support significant quality issues associated… more
- Genmab (Far Hills, NJ)
- …relationships with US thought-leaders based on mutual respect and reciprocal scientific information exchange related to medical therapies. This includes obtaining ... Global Medical Affairs programs, staying abreast of the evolving scientific & competitive landscape for relevant solid tumors Serve...program for solid tumor assets/disease and participates in the review of all US ISTs Ensures the delivery of… more
- Sun Pharma (Taro Pharma) (Billerica, MA)
- …Monitors and evaluates systems, equipment, records and trends data. Review /revise documentation (ie SOPs). Works under limited supervision following established ... EstimateUp to 5% Education and Job Qualification BS in a related scientific major required Good oral and written communication skillsAbility to follow specific… more
- Genmab (Princeton, NJ)
- …development of publications including extenders and enhanced content. Develop scientific content deliverables (including but not limited to, scientific ... agency/vendor partners to ensure timely delivery of quality content; provide direction, review developed content, and ensure process and content is consistent with… more
- Genmab (Pennington, NJ)
- …serious diseases by combining deep antibody expertise with unique methods of scientific discovery. We focus exclusively on antibodies, putting our deep understanding ... We're at the forefront of merging deep antibody expertise with groundbreaking scientific discovery, focused on transforming patient care. Dive into the dynamic world… more
- Genmab (Princeton, NJ)
- …working on projects with good understanding of the disease/ scientific /functional area and health authority acceptability. Responsibilities Compound/Indication Level ... main point of contact related to Statistics for designated compound/indication Follow scientific and technical progress within the field of biostatistics in drug… more
- Genmab (Cranbury, NJ)
- …accountable for the medical oversight of one or more clinical trials, medical review and communication of data, and medical input into regulatory documents, and ... and execute publication and clinical communication strategy in coordination with Scientific Communications Provide input to key external presentations Ensure career… more
- Genmab (Remote, OR)
- …all document types and regulatory submissions, including facilitating document contributor/ review meetings, developing and managing timelines, coordinating document ... digital capabilities. Lead, and actively contribute to, the development, review , implementation, and improvement of departmental processes, policies, standard… more
- BAEBIES INC (Durham, NC)
- …reviews, and product release. Roles and Responsibilities-- Utilize basic scientific principles, practices and existing technologies.-- Quality Control Testing- ... to investigate discrepancies and solve problems.-- Quality Assurance Reviews- Perform QA review of products. Monitor and inspect products to ensure that quality and… more
- Novant Health (Charlotte, NC)
- …of the nation's 150 Best Places to Work in Healthcare by Becker's Hospital Review Recognized as Leaders in LGBTQ+ Healthcare Equality by the Human Rights Campaign ... optimal health or supports a peaceful death. The Registered Nurse utilizes best scientific evidence and compassion to assist the patient in navigating their health… more
- Genmab (Princeton, NJ)
- …and changes that may impact the company's products. Prepare and review regulatory submissions, including INDs, (s)BLAs for accuracy, completeness, and compliance ... regulatory agencies, professional societies, and key opinion leaders. Participate in review of and comment on regulatory guidance as relevant. Drive continuous… more
- Genmab (Princeton, NJ)
- …teams for US/global health authority meetings. Participate in the development and review of submission documentation to support successful INDs/CTAs as well as ... agencies, professional societies, and key opinion leaders, as relevant. Participate in review of and comment on regulatory guidance as relevant. As assigned by… more
- Lincoln Memorial University (Cumberland Gap, TN)
- …Manipulative Medicine will be directly responsible for teaching, clinical duties, and scientific scholarship. They shall be held accountable for teaching the skills ... of the individuals identity, credit information, motor vehicle driving record, review of an individuals criminal conviction record (if any), verification of… more
- Genmab (Yardley, PA)
- …biomarker strategy and toxicologic pathology for a variety of antibody therapeutics. Scientific curiosity, strategic thinking, and the capacity to work well in ... clinical biomarker programs. Perform, as needed, primary reads and/or peer review of pre-clinical toxicology studies, including tissue cross reactivity studies,… more
