📑 Roles & Responsibilities: Direct accountability for the development and execution of strategic publication plans aligned with medical strategies and objectives. Track existing publication plans to ensure alignment with established medical strategies and objectives.Provide education to th ...
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📑 Title: Technical Project Coordinator Duration : 6+ Months.Location: Parsippany, NJ.Rate: OpenRequirementsJob Description :Strong Master Data and Customer Relationship Data Management Solution Architect to collaborate with both Veeva and the Analyti ...
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📑 Regulatory Clinical Trials Veeva Consultant Onsite at Tarrytown, NY 10591 Full Time OR 12 Months Contract It's a Banking Client. Main Skills: Veeva vault platform Gxp and non Gxp Key responsibilitie ...
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📑 Responsibilities: Collaborate with project team members to architect solutions per Business Requirements. Perform analysis and design (functional/non-functional) activities to create clinical/Regulatory solution landscapes for our Life Sciences Clients. Take complex concepts a ...
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📑 Job Description: The Benchtop Support specialist position will be responsible for providing IT support in our Digital Plant organization working to support, enhance, and maintain compliance for the GxP benchtop systems and instrumentation as well as site and global applications used within the manufacturing, quality, ...
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📑 Axsome Therapeutics, Inc. is a biopharmaceutical company developing and delivering novel therapies for the management of central nervous system (CNS) disorders. The Axsome team is a lean, dynamic group of individuals committed to addressing unmet needs for patients with CNS disorders. Axsome is based in New York City.About This RoleAxsome T ...
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📑 As the only global provider of commercial solutions, IQVIA understands what it takes to deliver nationally and internationally. Our teams help biopharma get their medicines to the people who need them. We help customers gain insight and access to their markets and ultimately demonstrate their product's value to payers, physicians and patients. A si ...
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📑 Job Description: Provide Data and Business analysis support to the Enterprise Master Data Management organization focusing on Customer Master.Data Analysis Support for Ex-US Next Gen Customer Master: Works independently on large volume data sets, data analysis and comparison be ...
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📑 Axsome Therapeutics, Inc. is a biopharmaceutical company developing and delivering novel therapies for the management of central nervous system (CNS) disorders. The Axsome team is a lean, dynamic group of individuals committed to addressing unmet needs for patients with CNS disorders. Axsome is based in New York City.About This RoleAxsome T ...
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📑 Do you want more than just another job? Are you ready to team up with an organization that values your contributions? Then Hired by Matrix is for you!Working with some of the US’ premier companies, we excel at connecting candidates with positive cultures and dynamic teams. We even go the extra mile with our signature Consultant ...
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📑 Highly reputable hedge fund in New York seeks Equities Analyst to support Portfolio Manager/Partner, head of the Biotech investment team.Group covers both public and private biotech companies research and investments.Among this multi-strategies fund's top operations, this team's investments in biotech domain range from mid to long term, public as w ...
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📑 Elevate Your Patent Career: Unique Opportunity for Biotech Patent Agents at Top Law Firm - Powered by MNF Global, Your Gateway to Excellence in IP, Patent, and Tech LawOverview:This dynamic law firm is seeking an experienced Biotech Patent Agent from a top U.S. law firm with a superb biotechnology and life sciences ...
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📑 Director of CommercializationWe are looking for a motivated and experienced individual with experience in life science/biotechnology commercialization, entrepreneurship, and grant writing. The ideal candidate should possess strong analytical and project management skills; an autonomous work ethic; initiative; and the ability to lead in an entre ...
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📑 Highly reputable hedge fund in New York seeks Equities Analyst to support Portfolio Manager/Partner, head of the Biotech investment team.Group covers both public and private biotech companies research and investments.Among this multi-strategies fund's top operations, this team's investments in biotech do ...
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📑 Job Description The Manager, Regulatory Review is responsible for ensuring regulatory submissions follow the protocols established by our pharmaceutical and medical/surgical device clients for promotional materials. This includes managing components of a submission package based on project type, experience working in ...
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📑 This is what you will do: The Field Reimbursement Manager (FRM) will be responsible for managing accounts in a specified region focusing on but not limited to Neurology. The FRM is responsible for providing access and reimbursement education to HCP office personnel including medical policies, prior authorization requirements, coding and billing, pr ...
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📑 ***This is a hybrid role with requirement to come into the NY Metro office 1 day a week on Wednesdays.***Are you passionate about being a critical part of the innovative biotech industry in an IR consulting capacity? If so, this is an exciting opportunity to work with a team with a long track record of providing best-in-class investor rel ...
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📑 Artia Global Partners OverviewArtia Global Partners LP is a multidisciplinary, healthcare focused investment firm.Artia Global employs a flexible, fundamental-oriented, and long-term investment approach. Our team pursues high conviction opportunities globally across all healthcare subsectors and the public / ...
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📑 Artia Global Partners OverviewArtia Global Partners LP is a multidisciplinary, healthcare focused investment firm.Artia Global employs a flexible, fundamental-oriented, and long-term investment approach. Our team pursues high conviction opportunities globally across all healthcare subsectors and the public / private spectrum. Artia Global’s flagshi ...
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📑 Position Summary: The Global Product Quality Specialist will be responsible for managing (and owning as needed) documentation and change controls associated with key deliverables to clinical and commercial documentation across multiple programs. Functional responsibilities include ...
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📑 Main Responsibilities include:• Supports delivery of projects involving implementation and/or management of Regulatory Information• Supports Data & Content Migration into Regulatory Information Management System, involves:o Source to target data model mapping< ...
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📑 Responsibilities: Supports delivery of projects involving implementation and/or management of Regulatory InformationSupports Data & Content Migration into Regulatory Information Management System, involves.Source to target data model mapping.Data quality assessment<b ...
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📑 Title: Manager, Site ComplianceAbout the role: Step into a crucial role within a large medical device company as the Manager of Site Compliance. We are in search of an experienced leader to lead all site Quality regulatory compliance activities, play a pivotal role in maintaining the effectiveness of the ...
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📑 Technical PM / Delivery Lead (TrackWise Digital)Location-Chatham ,NY(Onsite)Required Qualification/Skillset:Experience as Technical PM or Delivery Lead role on Quality Management System implementation projects (TrackWise Digital experience preferred. Can also consider o ...
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📑 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 can be a part of our teams achievements. Employing a global team of ...
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📑 Responsibilities: Sound understanding of Electronic Batch Records (EBR) and Review by Exception (RBE) and Recipe Authoring/Validation. Ability to work extended hours or a modified work schedule to assist manufacturing operations support model, including 12x7 on-call support rotation <b ...
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📑 When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance ...
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📑 SummaryMeet is proudly partnered with a well recognized healthcare communications agency looking for a VP-level candidate for their high-performing healthcare PR practice.The ideal candidate will have the ability to uphold responsibility for multiple client accounts, responsible for various strategic communications plans, corporate communications, ...
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📑 Catalio Capital Management is a New York City-based multi-strategy investment firm that invests in life sciences & healthcare companies through its private equity, private credit and public equities strategies. Today, we have a team of over 40 people between our NYC and London offices. Catalio is a close-knit and highly energetic team of smart and ...
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📑 Position: Quality Manager, Clinical Supply Chain QualityLocation: New Brunswick, NJDuration: 12+ Months (Extendable) Projected for 06 months and beyond depending on the business need. This Position is onsite Pay Rate: $41.60/hr on W2 Paid weekly Client: PharmaBenefits:401K, Paid-Time Off are NOT offered (except where state applicable sick time is r ...
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📑 100% onsiteJob Title: Quality Manager, Clinical Supply Chain QualityJob Description –The primary responsibility of this role is to ensure quality oversight and compliance with GMPs and GDPs (Good Distribution Practices) for Clinical Supply Chain Logistics. The role will be aligned with Global Quality and Logistics, necessita ...
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📑 Job title: CMC Regulatory Technical Writer IILocation: Bridgewater, NJ, HybridDuration: 1 yearSHIFT SCHEDULE 1st shift, 9-5 EST Mon-FriPay Rate starts: $47/ HOURHM Notes:* Hybrid - onsite Tuesday & Thursday - This can change at any time.* 5 years experience with scientific background (BA/BS, MS or PhD)* M ...
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📑 Role: Commercial Business Advisory ConsultantType: ContractContract Location: Princeton, NJ (onsite, locals only)Contract Duration: 11 monthsResponsibilities:In a Pharma Commercial IT advisory role, person should have the below skills:<br / ...
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Great News! We have discovered exciting live Veeva biotech job opportunities in New orleans just for you at American Jobs. You can even download the search results for Veeva biotech jobs in new orleans here.
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