Ich Q10 Jobs in Others

Director of BiostatisticsExperienced biostatistician who will be responsible for leading, developing and implementing statistical solutions to optimally support all phases of clinical trials and decision making. The successful candidate will function as a lead statistician across assi More...

ATTP Consultants Experience with Pharma industry Global Track and Trace Serialization system realization and deployments, including hands-on experience implementing SAP ATTP Understanding of global serialization regulations and experience installing, configuring, deploying, document More...

Senior Director, Clinical OperationsContract to PermPosition DescriptionPrimary ResponsibilityManage end-to-end enrollment process between research sites and CompanyResponsible for collection and review of screen data in a time-sensitive fashion that does not prolong the screening pr More...

About Company Company is a clinical-phase company. Our core technology combines proprietary dry-powder inhaler device technologies and advanced particle engineering-based inhaled drug formulation approaches to develop novel therapeutics that deliver the drug more directly to the lu More...

JOB SUMMARY: ToxicologyThe candidate will provide scientific oversight and strategic guidance for nonclinical safety evaluation programs from late-stage research through all phases of the drug development process including market application. reporting to the Senior Director Noncli More...

At Bristol Myers Squibb, we are inspired by a single vision transforming patients lives through (link removed) oncology, hematology, immunology and cardiovascular disease and one of the most diverse and promising pipelines in the industry each of our passionate colleagues contribut More...

At Bristol Myers Squibb, we are inspired by a single vision transforming patients lives through (link removed) oncology, hematology, immunology and cardiovascular disease and one of the most diverse and promising pipelines in the industry each of our passionate colleagues contribut More...

Solid medical knowledge, with CNS and oncology experience preferred.2+ years of experience as a field CRA.Requires 40% of travel within USAdvanced understanding of clinical development, knowledge and experience in international and local (FDA, ICH, etc.) requirements.

Amazing opportunity for a Regulatory Affairs Professional or even someone with a PharmD and Phd and Research experienceLevel of the role can be from Manager level to Associate Director, RA StrategyRegulatory AffairsParamus NJ (Hybrid; 2-day/week onsite)Job SummaryResponsible for devel More...

PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements. Our goal is to skyrocket our clients success, and you More...

Santa Monica, CA Contract Duration: 12-18 months Rate: Negotiable Responsibilities: Excellent employment opportunity for a Clinical Trials Management Associate I in the Santa Monica, CA area. May assist in the review of study-related or essential study start- More...

GROW WITH US:In Tandem means together, and we strive to embody that in every aspect of our business. Whether youre office-based or fully remote, Tandem Diabetes Care creates new possibilities for people living with diabetes, their loved ones, and the healthcare providers supporting th More...

GROW WITH US:In Tandem means together, and we strive to embody that in every aspect of our business. Whether youre office-based or fully remote, Tandem Diabetes Care creates new possibilities for people living with diabetes, their loved ones, and the healthcare providers supporting th More...

Responsibilities: Executes the commissioning, qualification, requalification, validation and any associated maintenance activities within the plant Manages multiple and complex CQV projects, provides status reports and coordinates with other departments or outside contractors/vendo More...

Director or Associate Director, Clinical Operations (DOE)The Director (or The Associate Director- DOE) of Clinical Operations is responsible for managing clinical operations activities at the project level including coordination of clinical trial activities, directing and supporting t More...

At Bristol Myers Squibb, we are inspired by a single vision transforming patients lives through (link removed) oncology, hematology, immunology and cardiovascular disease and one of the most diverse and promising pipelines in the industry each of our passionate colleagues contribut More...

Our client seeks a Clinical Research Operations professional to plan their Phase I Clinical TrialsRequirements Bachelors Degree in life sciences or healthcare field. Additional coursework in clinical trial design.Ability to travel as required (up to 25%).12+ years of proven experience More...

Manager of Regulatory Affairs in Somerset NJ.Fast growing company with great management team. Good writing and communication skills are requiredCMC experience required Experience with ANDA/IND/NDA preferredExperience with eCTD submissionsAnnual reports in accordance FDA and ICH guide More...

Senior Regulatory Associate in Somerset NJ.Fast growing company with great management team. Good writing and communication skills are requiredCMC experience required Experience with ANDA/IND/NDA preferredExperience with eCTD submissionsAnnual reports in accordance FDA and ICH guidance More...

Regulatory PublisherFast growing company with great management team. Good writing and communication skills are requiredCMC experience desired Experience with ANDA/IND/NDA preferredExperience with eCTD submissionsAnnual reports in accordance FDA nd ICH guidanceKnowledge and experience More...