Perform administrative functions in the Veeva CRM including activities such as maintaining user accounts, loading data reports, resolving end-user technical issues and monitoring system performance and utilization.
The purpose of this position is to lead and provide supervisory oversight to production areas for the sterile production of liquid injectable, sustained- release pharmaceutical products under cGMP regulations.
Assist in the development and maintenance of scientific communications materials including materials and tools for medical field force, including medical education; collaborate with key stakeholders on congress planning, provide congress intelligence, and create materials to support relevant communications.
Develops, updates and reviews relevant, unbiased medical information response documents and product profiles that are provided to customers and ensures content represents the most current, complete, medically accurate, evidence-based and scientifically balanced information.
Pacira Pharmaceuticals • Midwest and 5 other locations
Conduct site visit, site training and on-site case observation; document the on-site case findings, communicate with the investigators any technical issues identified during the site visit and follow up after the visit to ensure the closure of the issues.
The purpose of this position is for conducting and providing mechanical expertise in the maintenance and repair activities of the manufacturing and facilities equipment and systems in support of scheduled production activities and resolving the day-to-day equipment and facilities related issues.
Utilize advanced knowledge of aseptic pharmaceutical or biotech design, construction, installation, commissioning and validation to oversee Process, Clean-in-Place and Steam-in Place design, and Piping and Instrumentation Diagram development for clinical and commercial pharmaceutical facilities.
Build and implement innovative tools which would include personal and non personal solutions to enhance customer engagement; identify new opportunities, set objectives, define strategies and resources needed to achieve financial and strategic goals.
The Senior Director, Health Outcomes and Value Assessment will be responsible for developing health outcomes and access strategies, research studies, training and communicating clinical, reimbursement value and outcomes assessment in surgical pain management to senior level executives and health care researchers at key global and US national and regional health care executives across industry organizations, including managed care, pharmacy, IDN's, medical groups, payers, employers, patient advocacy organizations and healthcare policy opinion leaders.
The Sr. Clinical Trials Manager is responsible for the execution and delivery of all aspects of assigned clinical trials. The Sr. CTM participates in the design of clinical development plans, clinical trial synopses and clinical trial protocols.
Responsible for daily raw materials laboratory operations including trending, scheduling, staffing, training and troubleshooting to ensure all operations are in full compliance with established Standard Test Methods, compendial methods, vendor methods and safety guidelines.
Screen and analyze potential collaborations, license and acquisition opportunities from a scientific, medical, commercial and strategic perspective; develop and present compelling scientific and commercial rationales around potential transactional related activities.
Pacira Pharmaceuticals • Orlando, FL and 3 other locations
Support the educational and training needs of HCPs including providing additional education in response to unsolicited requests; providing surgical support, providing account education, facilitating development and implementation of individual institution needs/protocol, and appropriate scientific exchange.
Develops regulatory strategies and identifies and implements appropriate submission strategies for assigned projects. Provides input for product labeling, advertisement and promotion, and clinical projects.
This position is responsible for accounting research, which includes researching and implementing new accounting standards, researching and applying GAAP and SEC requirements to new and unusual transactions, writing accounting white papers to support and document the Company's position, and providing guidance on accounting issues.
This position will also be responsible for proper medical evaluation/interpretation of assigned clinical trials. It requires an understanding of the therapeutic context of the clinical program and is able to discuss hypotheses with experts, investigators and other hospital staff.