Drug Safety Specialist
2 weeks ago
REQUIREMENTS:
- Bachelor's Degree in nursing, pharmacy, or other health care related profession or life sciences
- Must have direct experience with end-to-end Case Processing (data entry and quality review) of both Clinical Trial and Post-marketing ICSRs
- Advanced proficiency in Microsoft Office applications
- Exceptional organizational skills and attention to detail
- Ability to successfully and efficiently multi-task
- Excellent communication skills (written and verbal)
- Knowledge of common safety database systems
- Ability to work collaboratively in a team environment
-
Medical Director, Drug Safety
1 day ago
Cambridge, United States Biogen Full timeJob Description You could be just the right applicant for this job Read all associated information and make sure to apply.About This RoleThe Medical Director, Drug Safety is responsible for global pharmacovigilance for marketed and/or investigational products, including review and analysis of safety data from post-marketing sources and from clinical trials,...
-
Drug Safety Associate
2 weeks ago
Cambridge, United States The Fountain Group LLC Full timeCurrently seeking a Drug Safety Associate for a prominent client of ours. This position is located in Cambridge, MA. Details for the position are as follows: Job Description: Shift: Monday-Friday (hybrid depending on what is needed in the project) Pay: $50-$59.05/hr depending on experience. This is a temporary assignment...
-
Medical Director, Drug Safety
4 weeks ago
Cambridge, Massachusetts, United States Biogen Full timeJob Description About This Role The Medical Director, Drug Safety is responsible for global pharmacovigilance for marketed and/or investigational products, including review and analysis of safety data from post-marketing sources and from clinical trials, the identification, and investigation of safety signals, management of benefit-risk profile for...
-
Senior Manager, PV
1 week ago
Cambridge, United States The Steely Group Full timeJob DescriptionJob Description*HYBRID OPPORTUNITY, ON-SITE ROUGHLY 3 AYS A WEEK DURING CORE HOURS* This Senior Manager-level role oversees the effective delivery of and continued evolution of Pharmacovigilance (PV) activities related to the organization’s clinical development programs. The Purpose of this Role:Develops and designs pharmacovigilance...
-
Cambridge, United States Massachusetts Institute of Technology Full timeLABORATORY SAFETY SPECIALIST, Environment, Health and Safety (EHS) Office, to support MIT's academic and business objectives by serving as an integral member of a multidisciplinary EHS office that serves the whole MIT community, and coordinate aspect Safety Specialist, Laboratory, Health, Safety, Specialist, Office, Healthcare, Education
-
Director of Drug Substance Manufacturing
4 weeks ago
Cambridge, United States QurAlis Full timeABOUT THE COMPANY QurAlis is a clinical-stage biotechnology company developing breakthrough precision medicines for amyotrophic lateral sclerosis (ALS) and other neurodegenerative diseases with genetically validated targets. QurAlis is trailblazing the path to conquering amyotrophic lateral sclerosis (ALS) and other neurodegenerative diseases with...
-
Director of Drug Substance Manufacturing
3 weeks ago
Cambridge, United States QurAlis Full timeABOUT THE COMPANY QurAlis is a clinical-stage biotechnology company developing breakthrough precision medicines for amyotrophic lateral sclerosis (ALS) and other neurodegenerative diseases with genetically validated targets. QurAlis is trailblazing the path to conquering amyotrophic lateral sclerosis (ALS) and other neurodegenerative diseases with...
-
Director of Drug Substance Manufacturing
4 weeks ago
Cambridge, United States QurAlis Full timeABOUT THE COMPANY QurAlis is a clinical-stage biotechnology company developing breakthrough precision medicines for amyotrophic lateral sclerosis (ALS) and other neurodegenerative diseases with genetically validated targets. QurAlis is trailblazing the path to conquering amyotrophic lateral sclerosis (ALS) and other neurodegenerative diseases with...
-
Environmental Health Safety Specialist
4 weeks ago
Cambridge, United States Randstad Life Sciences US Full timeImmediate opportunity for an Environmental Health & Safety Specialist II to work with multi-national pharmaceutical company dedicated to pharmaceutical research and vaccine development. The HSE Associate Level Service Provider serves an important and highly visible role helping to ensure that site HSE Management System (HSE-MS) requirements are appropriately...
-
Environmental Health Safety Specialist
3 weeks ago
Cambridge, United States Randstad Life Sciences US Full timeImmediate opportunity for an Environmental Health & Safety Specialist II to work with multi-national pharmaceutical company dedicated to pharmaceutical research and vaccine development. The HSE Associate Level Service Provider serves an important and highly visible role helping to ensure that site HSE Management System (HSE-MS) requirements are appropriately...
-
Environmental Health Safety Specialist
4 weeks ago
Cambridge, United States Randstad Life Sciences US Full timeImmediate opportunity for an Environmental Health & Safety Specialist II to work with multi-national pharmaceutical company dedicated to pharmaceutical research and vaccine development. The HSE Associate Level Service Provider serves an important and highly visible role helping to ensure that site HSE Management System (HSE-MS) requirements are appropriately...
-
Associate Medical Director, Drug Safety
3 weeks ago
Cambridge, Massachusetts, United States Biogen Full timeJob Description What you’ll do: The Associate Medical Director, Global Safety Physician will be responsible for global pharmacovigilance for investigational and/or marketed products, including review and analysis of safety data, design of clinical trials, identification and investigation of safety signals, management of benefit-risk profile for assigned...
-
Safety Specialist
4 weeks ago
Cambridge, Massachusetts, United States QData Full timeRoles & Responsibilities Monitor manage and ensure delivery of projects in a deadline-driven environment. Author Technical SDLC deliverables Technical assistance for testing preparation and implementation of enhancements Contribute to the creation of operational support documentation Drive technical delivery and accountability of internal staff as well as...
-
Environmental Health
2 weeks ago
Cambridge, United States Regal Rexnord Full timeThe Environmental Health & Safety Intern will help oversee multiple projects/facilities within the plant for environmental compliance and sustainability. The chosen candidate must have good time management skills and the ability to prioritize project needs for an efficient operations schedule.The Environmental Health & Safety Intern will provide support and...
-
Safety, Regulatory,
2 weeks ago
Cambridge, United States Growmark, Inc. Full timeUnder the direction of the Operations Manager, is responsible for implementation and coordination of Safety, Regulatory, and Environmental compliance, and accident prevention programs for Gold Star FS. ESSENTIAL JOB FUNCTIONS Implements EHS (Environm Environmental Specialist, Regulatory, Environmental, Operations Manager, Bridge, Safety, Manufacturing,...
-
Research Specialist, Koehler Lab
2 weeks ago
Cambridge, United States Massachusetts Institute of Technology Full timeRESEARCH SPECIALIST, Koch Institute (KI) for Integrative Cancer Research-Koehler Lab, to impact medicine by expanding the repertoire of druggable targets and developing new technological solutions to solve bottlenecks in the drug discovery process. T Research, Specialist, Chemistry, Research Fellow, Technology, Education, Application
-
Senior Regulatory Affairs Specialist
6 days ago
Cambridge, United States Validation Associates Full timeContract Role:Schedule: It will be on average 20 hours per week, preferably 4 hours a day M-F, but we can be flexible depending on the candidate.-REMOTE- Regulatory Affairs Specialist DS Process Expert with NDA filing experience.May September (20 hours week)Contractor to support regulatory documentation review for the Drug Substance part of the NDA...
-
Environmental Health
2 weeks ago
Cambridge, MD, United States Regal Rexnord Full timeThe Environmental Health & Safety Intern will help oversee multiple projects/facilities within the plant for environmental compliance and sustainability. The chosen candidate must have good time management skills and the ability to prioritize project needs for an efficient operations schedule.The Environmental Health & Safety Intern will provide support and...
-
Senior Regulatory Affairs Specialist
1 week ago
Cambridge, United States Validation Associates Full timeContract Role: Schedule: It will be on average 20 hours per week, preferably 4 hours a day M-F, but we can be flexible depending on the candidate. -REMOTE- Regulatory Affairs Specialist DS Process Expert with NDA filing experience. May – September (20 hours week) Contractor to support regulatory documentation review for the Drug Substance part of the NDA...
-
Safety Specialist
4 weeks ago
Cambridge, United States QData Full timeRoles & Responsibilities Monitor manage and ensure delivery of projects in a deadline-driven environment. Author Technical SDLC deliverables Technical assistance for testing preparation and implementation of enhancements Contribute to the creation of operational support documentation Drive technical delivery and accountability of internal staff as well...