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ROLE SUMMARY Develop, negotiate, track and execute North American Clinical Study Agreements with institutions and investigators participating in sponsored clinical trials. Work with internal and ...
Shift Timings: 8:00 AM - 5:00 PM Recent grad with packaging degree would work Important updates from the manager Industry or academic experience would be highly preferred Experience ...
The Clinical Trial Registration Associate will prepare and provide operational support for the registration of clinical trials into US database (ClinicalTrials.gov).Detailed Position ...
Support Medical Safety Assessment Physicians (MSAP) in leading Safety Data Review (SDR) Teams. Appropriately perform core signal detection activities, elevate program or portfolio issues impacting ...
The Compound Management Consultant will be responsible for the execution of the day to day procedures necessary to facilitate compound request fulfilment and other inventory management ...
Shift Sunday - Wednesday 1st ShiftPerform operations necessary for quality testing and plays a role in implementing new technology within quality control. At more senior levels, provide an ...
Research Associate III to join our Developability & Preformulation Sciences (DPFS) group. DPFS is part of the global Biologics Drug Product Development organization, a critical R&D function ...
Description: CORE JOB FUNCTION(S): Use current (or new) techniques to address questions of drug mechanism of action, drug differentiation and drug sensitivity/resistance Set up ...
Job Title: Laboratory Technician IIJob responsibilities description: Effective communication on issues and solutions Plan and perform routine tasks competently and independently within a timely ...
Navigational support for developing and driving the GRO TSA exit strategy TSA support for cross functional TSA exit planning, execution and oversight Assist with developing Viatris governance ...
Bring Your Own Device (BYOD)/LaptopResponsibilities:Propagate tissue culture for the scientific staff Carry out in vitro assays as requestedLab organizationWashing glassware, preparing media, ...
Serves as the subject matter expert for Medical Information (MI) on responsible product(s) and associated therapeutic area(s) Exhibits comprehensive knowledge of MI work and processes as well as ...
Important Updates from the managerLocal candidates needed2 days a week they would be working onsite and rest remote during pandemicDomestic travel is involved in this role after pandemic10 - 20 ...
Remote until COVID-19 restrictions are liftedThe Scientist will be responsible for supporting in generation of high-quality functional similarity packages that meet the expectations of global ...
ROLE SUMMARY Client’s Cell Line Development (CLD) organization is seeking a motivated, qualified candidate to be a technical leader, in a lab-based Scientist role. The successful candidate ...
Responsible for general laboratory and operational support. Including providing logistical support for samples and compounds management, ordering supplies and carrying out general bench work ...
Responsibilities• Supports a high performing, cross-functional global communications matrix team engaged in the planning, integration, and execution of HEOR publication activities globally• ...
Responsilbities:• Participates in various and assigned phases of Quality Control testing to support production, method validation & stabilityo Visual evaluation of vials, syringes, plates, ...
The CQ Investigator is responsible for completing Laboratory investigations, providing documented evidence of root cause and Corrective and Preventative Actions for stability laboratory issues. This ...
Qualifications Required: Capable of exchanging straightforward information, ask questions, and check for understanding. Must be proficient in Microsoft Office Suite and relevant clinical ...
