Mgr, Research I New Jersey
7/14/2015 1:37 PM

The Research Manager is a scientific leader and key member of the management team in AD, overseeing the work and professional development of a significant group of scientists. The Research Manager has knowledge and expertise in analytical testing of raw materials and/or pharmaceutical products, and is able to lead ANDA project work from initial development through the ANDA filing stage and beyond  ...View Job
Director, Health Economics and Outcomes Research New Jersey
7/14/2015 1:34 PM

The role of the Director is to develop and execute health economics and outcomes research strategies to optimize the reimbursement and access of Forest products in one or more therapeutic areas. May also manage direct reports as assigned. Qualifications: 1. Develop value and outcomes strategy, plans, and budget for Forest brands and early stage products (life cycle strategy). 2. Design, plan  ...View Job
Senior Statistical Programmer New Jersey
7/14/2015 1:30 PM

The role of the Senior Statistical Programmer is to perform statistical programming activities for all assigned Phase I-IV clinical studies sponsored by Forest Research Institute (FRI) and its partners. This position performs statistical programming for clinical studies, integrated summaries, and in support of responses to requests from regulatory authorities. This position serves as a study lead   ...View Job
Director Clinical Program Management New Jersey
7/14/2015 1:28 PM

This position supports the Director, Clinical Program Management, in the strategic interface between Clinical Development (CD) and a cross functional team at the program/study level. This position helps guide the integration of scientific objectives with standard operational processes to ensure the delivery of scientific content (e.g. as defined in CDP), throughout the program’s lifecycle. The may  ...View Job
Director, Portfolio Management New Jersey
7/14/2015 1:21 PM

Position Summary: The Director, Portfolio Management will be responsible for identifying and evaluating new product candidates for addition to Actavis’ US Generics pipeline, ensuring that selected products are aligned with the overall portfolio strategy and functional processes and that the right products, dosage forms and technologies are being evaluated and selected. Focus will be on high-value  ...View Job
Manager, Publications New Jersey
7/14/2015 1:19 PM

The Publications Manager will oversee development of strategic publication plans and analyses for multiple therapeutic areas or indications. Ensures globalization of publication plans under their purview resulting in global publication plans. Represents the publications perspective on post-approval teams (PATs) providing therapeutic area (TA) and publications knowledge to guide the team’s decision  ...View Job
Sr. Scientist Drug Safety Information Management New Jersey
7/14/2015 1:17 PM

The Sr. Scientist in the PVRM Safety Information Management group is responsible for creating internal safety surveillance documents as well as safety reports for regulatory authorities for the company products, handling internal ad hoc queries/reports, analyzing/summarizing complex safety data, managing the operations of Safety Management Team (SaMT) meetings, managing signal detection activities  ...View Job
Safety Information Coordinator New Jersey
7/14/2015 1:15 PM

Position Summary The Safety Information Coordinator receives all non-telephonic incoming safety information, evaluates, compiles and qualifies the information for completeness, confirms receipt with Associated Business Partners (ABP) when applicable, and prepares for triage. Determines when one of the four essential criteria is missing and conducts follow-up with the reporter. Reviews case inform  ...View Job
Medical Reviewer, Patient Safety Operations New Jersey
7/14/2015 1:12 PM

Position Summary: The Medical Reviewer applies medical expertise and provides guidance for individual case safety report (ICSR) assessment, quality and reporting to ensure patient safety and achieve compliance with corporate and departmental Standard Operating Procedures (SOPs), global regulations. Responsible for medical review and safety surveillance of ICSRs, for development and marketed prod  ...View Job
Senior Director, Clinical Development New Jersey
7/14/2015 1:06 PM

This position serves the Clinical Asset Lead (CAL) for a complex asset (e.g. with multiple development programs) or group of assets. In this capacity, the CAL is single point of accountability for clinical development strategy and plan, including design and delivery of all clinical programs for the asset(s). The position partners with the Therapeutic Area Head (TAH) and Director of Clinical Pro  ...View Job