- Merck & Co. (North Wales, PA)
- …Empathy, Global Strategy, Hematology, Interpersonal Relationships, Medical Affairs, Medical Research, Medical Writing, Medication Safety , Partnership ... Job Description Role Summary: The Global Senior Director Medical Affairs (GDMA) is a subject matter expert...in collaboration with RDMAs, while also serving as a review panel member on TA specific MISP's to support… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Patient Safety , with cross-functional working relationships within Case Processing, Medical Review , Submissions and Compliance and the centralized teams (eg, ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk...for overseeing and ensuring efficient operations for the Patient Safety Call Center, Intake and Triage, Customer Care Call… more
- Merck & Co. (Rahway, NJ)
- …quality and compliance in a regulated environment.- - Key responsibilities: - Enter, review , approve, and submit individual case safety reports for assigned ... Management, Compliance Investigations, Data Analysis, Data Management, Detail-Oriented, Drug Safety Surveillance, Employee Training, Learning Management Systems (LMS), Management… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... rare diseases and immune disorders. Job Summary: The Sr. Director, Clinical Safety MD, will lead the development and implementation of integrated project/product… more
- Aequor (Thousand Oaks, CA)
- …processes . Case processing experience. Attention to detail. Competence in Argus safety systems and medical coding. Comprehensive English writing skills. ... Initial 4 month contract with possible extension Purpose: To support the safety surveillance process for products by performing follow up activities with patients… more
- Lupin Pharmaceuticals (Coral Springs, FL)
- …Monitoring: Provide medical oversight during clinical trials to ensure participant safety and data integrity. Review and interpret safety signals, adverse ... OverviewThe Respiratory Clinical Development Medical Lead will oversee the clinical and medical aspects of new respiratory medicines, including new drug or… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... immune disorders. Job Summary: Reporting to the Sr. Director, Medical Affairs QA, the Director of Medical ...conduct quality reviews of product profiles, ensuring thorough management review of all quality and compliance topics, including Key… more
- CHRISTUS Health (Palestine, TX)
- …Jesus Christ by caring for critically ill and injured persons in the air medical environment. Practice is carried out with a high degree of independence in ... and involves interacting with a wide range of healthcare and public safety professionals in stressful situations. The position also requires subject matter… more
- CHRISTUS Health (Texarkana, TX)
- …policy to provide expected patient outcome and documents in the medical record accordingly. Responsibilities: Demonstrates appropriate hand hygiene, use of PPE, ... departmental policies.Operates all available dialysis equipment and supplies based on safety , effectiveness, and cost in accordance with hospital and departmental… more
- Geisinger (Scranton, PA)
- Job Title: RN - Graduate Registered Nurse (Geisinger Community Medical Center, Scranton)Location: Scranton, PennsylvaniaJob Category: Inpatient RN - Registered ... here to learn more about the units belowAdvanced Acute Care ( Medical & Oncology, Surgical Trauma, Cardiac/Telemetry, Orthopedics)Cardiac Special Care UnitChildbirth… more
- Merck & Co. (Millsboro, DE)
- …large scale vaccine manufacture, and animal studies.This position sits within the Global Safety & Environment organization, and reports to the Associate Director of ... Safety & Environment at Millsboro, DE.Responsibilities:Ensure compliance with internal...federal, state, and local biosafety regulations, and advise management accordingly. Review risk assessments for biological materials and laboratory operations… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …generation strategies and activities as part of the USOMA Plan. Provides medical review of expanded access programs (EAP) and, investigator-initiated studies ... of a US IIS Review Committee, for assigned compound. Collaborates with Global Medical Affairs and across USOMA functions to develop, review , and align on key… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …systems to improve business effectiveness.Read and interpret documents such as safety rules, operating instructions, and logbooks. Review and provide feedback ... provide guidance and determine immediate path forward for manufacturing quality issues. Review of all documentation, in accordance with Good Documentation Practices… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …generation strategies and activities as part of the GMA Plan. Provides medical review of expanded access programs (EAP) and, investigator-initiated studies ... develop, review , and align on key scientific communications and medical information response documents within legal and compliance regulations. Leads internal… more
- Merck & Co. (Rahway, NJ)
- …closely with team members and partner groups including formulators, engineers, Quality, Safety , and Facilities management to drive overall success and performance of ... with all applicable internal and external regulations for quality (GMP), safety , etc.Attention to Detail: Maintain meticulous records of formulation processes,… more
- SolutionHealth (Nashua, NH)
- …process.Assist surgical team with intra-operative procedures and with closure procedures. Review the surgical booking and matches procedures to preference ... preference cards for selection of instrumentation.Inspect instruments for sterility, safety and function.Evaluate surroundings to maintain sterile field.Who You Are:… more
- AUROBINDO (Dayton, OH)
- …Document work clearly and perform tests accurately.Prepare and/or review Test Procedures, SOPs, Validation Protocols/Reports as assigned.Perform maintenance ... with all regulatory/in-house requirements (may include but not limited to safety , housekeeping, laboratory chemical waste, cGMP, cGLP, documentation) when performing… more
- PhysEmp (North Andover, MA)
- …and safety concepts and OSHA regulationsGraduate of an accredited medical schoolAt least three years of post-residency clinical experienceMust be Board Certified ... for health care providers is requiredKnowledge and Skills:Ability to collaborate with both medical and non- medical staff (ie Safety Department, HR, Site… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …or final product samples submitted to the QC laboratories.Perform peer review /approval of laboratory data.Utilize electronic systems (LIMS) for execution and ... documentation of testing.Create, review and approve relevant QC documents, SOP's and WI's.Perform...and WI's.Perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements.Work in a… more
- Merck & Co. (Rahway, NJ)
- …as needed. The position is also responsible for implementing actions to meet Safety and Environment (S&E) and GMP requirements as well as ensuring facility readiness ... and/or support batch processing readiness and execution activities. Prepare, review , and/or approve GMP Documentation as appropriate. Author/Approve Standard… more
