49 Pharm./Biotech Job Openings Within 50 mi. of New York, NY

Displaying results 1 - 15 of 49
Green Key Resources

Contract Coordinator

Green Key Resources - East Hanover, NJ
- Responsible for resolving contract processing issues, liaising with Req to Pay (RTP), Outsourcing Managers, Vendors and Finance Department. - The Contract Coordinator may be responsible for drafting and/or procuring and processing partially executed contracts, amendments and agreements. - The main point of contact, tracks the process and ensures completion of each contra...
Posted Apr 24, 2014   —   Application Deadline: None
Green Key Resources

Clinical Project Manager

Green Key Resources - Long Island, NY
PRIMARY DUTIES: • Quote, plan, direct, and coordinate all activities of designated projects to ensure that goals and objectives of projects are accomplished within prescribed time frame    • Accountable for overall project management for assigned projects • Assigned role as primary customer contact.  Responsible for customer expectation management • M...
Posted Apr 24, 2014   —   Application Deadline: None
Green Key Resources

Clinical Research Manager II

Green Key Resources - East Hanover, NJ
- Support efforts in the planning, execution and reporting of USCDMA clinical trials in Oncology. - Implementation of clinical trials in the United States, within a cross functional team and with oversight from the Associate Director. - Interfacing with the hematology therapeutic area global and US clinical team members, clinical operations, scientific operations, regulato...
Posted Apr 24, 2014   —   Application Deadline: None
Green Key Resources

Expert Clinical Manager III

Green Key Resources - East Hanover, NJ
- Responsible for all operational aspects of 1 or more clinical trial(s) under the leadership of Clinical Trial Head (CTH). - Support all scientific aspects of clinical trial(s) as assigned. - Responsible for program level activities as assigned. - Ensure all operational trial deliverables are met according to timelines, budget, operational procedures and quality stan...
Posted Apr 24, 2014   —   Application Deadline: None
Green Key Resources

Medical Editor/Proofreader

Green Key Resources - Warren, NJ
- Proofread promotional materials to ensure error-free work, including checking for correct spelling, grammar, punctuation, format, size/specs, codes, disclaimer copy, and adherence to AMA and Client style. - Review materials at multiple stages of a job - art proofs, printer proofs, laser sign offs, interactive test files, etc. - Perform straight reads as well as proofread...
Posted Apr 24, 2014   —   Application Deadline: None
Green Key Resources

Global Pricing & Market Access Contractor

Green Key Resources - Summit, NJ
- Ownership of a disease - therapeutic class and informing of Pricing and Market Access potential in that disease state. - Identification of payer needs and anticipation of their reaction to lifecycle products. - Conduct of a gap analysis between payer expectations and what the product can deliver. - Development of a plan to address identified gaps through studies, pu...
Posted Apr 24, 2014   —   Application Deadline: None
Green Key Resources

Regulatory Document Specialist

Green Key Resources - Basking Ridge, NJ
- Ensures timely review of submission documents for proper formatting as well as publishes these documents, ensuring submission readiness. - Assists with developing and maintaining document formatting and publishing procedures and standards for regulatory submissions. - Assists with training staff on procedures and standards. - Becomes familiar with and assists in pro...
Posted Apr 24, 2014   —   Application Deadline: None
Green Key Resources

Associate Clinical Research Scientist

Green Key Resources - Basking Ridge, NJ
- Assisting with regulatory and/or IRB/IEC submissions, including document generation, collection and review. - Reviewing applicable study documents (e.g. Medical Monitoring Plans, Randomization Plans, Clinical Monitoring Plans, Data Management Plans, etc.). - Managing and tracking clinical trial supplies. - Managing clinical trial budgets and vendor/site payments.
Posted Apr 24, 2014   —   Application Deadline: None
Green Key Resources

Senior Data Manager

Green Key Resources - Ardsley, NY
- Participates in study planning and execution by contributing to the following activities in collaboration with Biostatistics and Clinical Operations: protocol review; case report form (CRF) design; CRF completion guidelines preparation; data management plan (DMP) development; database coding, transfer and edit check specifications review; user access testing (UAT) of electronic da...
Posted Apr 24, 2014   —   Application Deadline: None
Green Key Resources

Data Manager

Green Key Resources - Ardsley, NY
* Responsible for overseeing data management tasks from study start-up through database lock, for clinical trials. * Collaborates with the Clinical Project Managers (CPMs), Biostatistics team, and data management vendors to ensure database development, data review/cleaning, database auditing, database lock, and receipt of final database deliverables are in compliance with standard oper...
Posted Apr 24, 2014   —   Application Deadline: None
Green Key Resources

Statistical Associate Director

Green Key Resources - Suffern, NY
* Provide statistical support for the site and within the global network. *Provide statistical assessments and develop models for process improvements, process monitoring and process control purposes. * Actively be involved in troubleshooting and process validations activities, which includes adherence to regulatory and GMP requirements Qualifications * BSc...
Posted Apr 24, 2014   —   Application Deadline: None
Green Key Resources

Biostatistician III

Green Key Resources - East Hanover, NJ
- Designing clinical studies. - Writing and reviewing statistical sections and other relevant parts of study synopses and protocols. - Support study start up activities. - Develop RAP, program TLFs, preparation for database lock, dry run and CSR activities; review CRF, DB spec, VAP; support analysis as required for decision making at project level; support analysis an...
Posted Apr 24, 2014   —   Application Deadline: None
Green Key Resources

Medical/ Scientific Writer

Green Key Resources - Murray Hill, NJ
* Serve as the primary medical writing representative on project teams.   * Collaborate with personnel from clinical, regulatory and other scientific parties. * Manage the writing, editing and reviewing of diverse regulatory clinical documents including clinical protocols, clinical study reports, investigator brochures, informed consent forms, clinical data summaries and other cli...
Posted Apr 24, 2014   —   Application Deadline: None
Green Key Resources

Regulatory Specialist

Green Key Resources - Murray Hill, NJ
*Work in collaboration with other departmental and company representatives to ensure that all required reports and documentation are prepared and submitted on a timely basis.  *Responsible for the scheduling, timelines, follow-up, and preparation of all IND/NDA Annual Reports, Amendments, Briefing Documents and other periodic submissions in support of regulatory filings to regulatory a...
Posted Apr 24, 2014   —   Application Deadline: None
Green Key Resources

Senior Quality Engineer

Green Key Resources - New Brunswick, NJ
* Ensure quality and validation programs are well-defined, executable, meet customer and business needs, and are in compliance with regulatory requirements. * Implement global programs/policies/procedures with respect to Validation, Revalidation, Commissioning Qualification, Sampling Plans, Process Capability, Root Cause Analysis/Failure Investigations. * Proactively examines syst...
Posted Apr 24, 2014   —   Application Deadline: None
Displaying results 1 - 15 of 49