£100 - 125
Location: London, Remote
... problem-solving, organizational and communication skills Familiarity with 21 CFR Part 11, FDA, and GCP requirements. Proficiency with MS Office applications. Experience with Sales Applications: Dynamics ...
Company: Energy Vault
(1 week ago)
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£100 - 125
Location: Witney
... Systems (EMS), and other regulatory requirements. Complies with U.S. Food and Drug Administration (FDA) and international regulations, other regulatory requirements, Company policies, operating procedures, processes, and task ...
Company: Abbott
(1 week ago)
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£100 - 125
Location: Cambridge
... trials. Leading GCP inspection readiness activities and hosting regulatory GCP inspections (FDA, MHRA, EMA). Implementing and delivering risk-based clinical audit programmes. Establishing ...
Company: MoonLake Immunotherapeutics (NASDAQ: MLTX)
(1 week ago)
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£125 - 150
Location: London
... .g., NIST, OWASP, MITRE ATT&CK, PASTA, STRIDE) and standards such as FDA cybersecurity guidance Experience assessing security risks using industry standard methods ...
Company: Astro Studios, Inc.
(1 week ago)
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£100 - 125
Location: Cambridge
... medical terminology. Excellent computer skills. Excellent knowledge of GCP, ICH and FDA regulations. Ability to provide appropriate leadership to clinical sites and team members as appropriate ...
Company: Akebia Therapeutics
(1 week ago)
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£100 - 125
Location: Oxford
... . Ivonescimab was granted Fast Track designation by the US Food & Drug Administration (FDA) for the HARMONi clinical trial setting. Overview of Role: The Manager, Upstream MSAT, is ...
Company: Summit Therapeutics Sub, Inc.
(1 week ago)
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£100 - 125
... Sciences to be able to work in our organisation you must be aged 18 years or over and not have been debarred by the FDA. If you indicate you are under the age of 18 or have been debarred then ...
Company: Quotient Sciences Limited
(1 week ago)
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£100 - 125
Location: Cambridge
... , team management, and strategic planning skills. Track record of close interactions with FDA in the context of biologics and cell and gene therapies development. #J-18808-Ljbffr
Company: VCLS
(1 week ago)
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£100 - 125
Location: London
... (INDs), and Risk Management Plans. Act as a liaison with local HAs (e.g. FDA, EMA) as required. Ensure timely and effective responses to HA queries and requests. Collaborate ...
Company: Novartis
(1 week ago)
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£100 - 125
... the way in empowering consumers and patients to take care of their heart. Using our FDA-cleared medical-grade hardware and software, millions of users have taken more than ...
Company: AliveCor, Inc.
(1 week ago)
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£100 - 125
Location: London
... companion diagnostics for patient selection. Experienced in global health authority interactions (EMA, FDA, MHRA, CDE). Having participated or led a drug development program to successful registration ...
Company: BioNTech IMFS
(1 week ago)
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£100 - 125
Location: London
... respiratory sleep disorders. Our core product is the WatchPAT family, a revolutionary FDA-cleared portable home sleep apnea test device, that is based ...
Company: Zoll Medical Corporation
(1 week ago)
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£100 - 125
Location: London
... -performing clinical teams. Experience engaging with global regulatory bodies (e.g., FDA, Notified Bodies, PMDA). Excellent written and verbal communication skills, including executive ...
Company: Medtronic
(1 week ago)
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£100 - 125
Location: London
... Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across ...
Company: Syneos Health Careers
(1 week ago)
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£100 - 125
Location: Boston
... vendor relationships and functional service provider (FSP) partnerships In-depth understanding of FDA and ICH/GCP regulations and guidelines related to data capture and data management processes ...
Company: Kailera Therapeutics
(1 week ago)
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£100 - 125
Location: London
... . Bonus Points For Experience working in early-stage or rapidly scaling companies. Familiarity with FDA regulations and running trials in the US. A background in science, engineering, or regulatory affairs. Why ...
Company: Sava
(1 week ago)
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£100 - 125
Location: London
... : Ensure adherence to Good Clinical Practice (GCP), ICH guidelines, and regulatory requirements (FDA, EMA).? Industry Best Practices: Stay up to date with emerging trends and best practices in clinical ...
Company: Pop Science
(1 week ago)
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£100 - 125
Location: South Yorkshire
... and patients to develop a strong product pipeline to be manufactured at its CA, CE, ISO, US FDA approved facilities. At Clinisupplies, we want to make a difference in healthcare, that means ...
Company: Clinisupplies
(1 week ago)
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£100 - 125
... quality standards. Ensure clinical trial conduct aligns with ICH/GCP guidelines, FDA/EMA regulations, and internal SOPs. Partner cross-functionally with global teams, vendors ...
Company: Planet Pharma
(1 week ago)
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£100 - 125
Location: London
... . Ensure all molecular biology processes align with GMP, GLP, and regulatory expectations from the FDA, EMA, and other governing bodies. Represent the company in scientific conferences, regulatory discussions, and strategic ...
Company: CPL Healthcare
(1 week ago)
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