Archives

Contractor – NJ Candidate needs to have hands-on experience conducting all DM activities and possess strong project management and excellent interpersonal skills to independently manage a global project. Experience in InForm, Oncology a plus. Independently perform all data management functions to ensure timely and quality database lock for studies Phase I-III. Perform data management activities …

Contractor – NJ Perform SAS programming to provide data review complex listings/reports to support Data Management, Medical Coding, and other areas of Clinical functions for Oncology trials. Develop programs & graphs in JReview for easier data review and visualization. Develop programs for patient profiles and ad hoc reports to support the clinical teams for Oncology …

Sr. Regulatory Affairs Associate – Full-Time (2 open)      Based in New York City & San Francisco   Outstanding growth opportunity with a world-class global biopharmaceutical company focused on developing drugs for the treatment of a range of severe skin disorders. They have a  unique expertise in understanding the interaction of light and human skin, …

Medical Science Liaisons – 3 Open – NE, Central and SW Regions Outstanding opportunity with a multinational specialty pharmaceutical company who has a diverse product portfolio with focus on branded pharmaceuticals, branded generics and over-the-counter products. Specialization in dermatology, eye health, neurology and consumer healthcare. Be a part of this exciting Pharmaceutical Industry Leader! Duties …

Contractor – Northern NJ DUTIES:  This role will report to the Director of Program Management, Medical Affairs Summary: Coordinating activities associated with the development, execution and management of contract life cycle for the Clinical Operations and Medical Affairs department. Contract types include Confidentiality Agreements, Master Service Agreements, Clinical Trial Agreements, General Services Agreements, and Consulting …

Contractor – Northern NJ  DUTIES:   Person must have at least 5 years of both coding and clinical data review experience who can support one of our submissions. Responsible for the selection and review of appropriate codes of reported terms in clinical trials not limited to adverse events, medical history and medications. Ensures that the term …

Contractor  – Northern NJ  DUTIES:  To support the Biostatistics team by carrying out and conducting programming activities of statistical programmers, and coordinating with external vendors (as required), and to ensure timely and accurate programming and validation activities for clinical studies. Contributes to the overall efficiency and best practice running of the Biostatistics group, demonstrating the …

Contractor  – Northern NJ DUTIES:  Sr. Clinical Outsourcing Consultant (Sr. Manager Level)  Support Company’s  internal customers in the development of outsourcing requirements for Phase I-IV global clinical trials. Lead and support the qualification and evaluation process for new service providers. Lead the process of Request for Proposal (RFP) development from service provider selection through final …

Contractor  – Northern NJ DUTIES:  To provide professional services for ongoing administration and application support for Success Factors learning management system. Technical Skills: – Be able to perform administrator tasks – Understand roles and security required when developing or customizing new object – Add new fields to the employee profile and talent profile – Create …

 Contractor  – Northern NJ DUTIES:  Administrative Assistant: Expense Report Submission: Process travel and entertainment expense reimbursements using ADP Concur. Reconcile purchasing cards on a monthly basis.  Calendar Management: Advise others on colleagues’ availability for meetings. Arrange WebEx and teleconference calls via Lotus Notes. Arrange for catering or luncheons. Travel coordinator: Create Travel Approval Forms using …