Regulatory Documents Jobs in Waltham, MA
Regulatory Documents Jobs in Waltham, MA
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Your CareerThe Global Regulatory and ESG Compliance Manager will drive ESG programs within the supply chain focusing on human rights environmental standards and sustainable practices. This role includes staying current with global regulations conducting gap assessments and ensuring co More...
Not Disclosed
Your CareerThe Global Regulatory and ESG Compliance Manager will drive ESG programs within the supply chain focusing on human rights environmental standards and sustainable practices. This role includes staying current with global regulations conducting gap assessments and ensuring co More...
Not Disclosed
Your CareerThe Global Regulatory and ESG Compliance Manager will drive ESG programs within the supply chain focusing on human rights environmental standards and sustainable practices. This role includes staying current with global regulations conducting gap assessments and ensuring co More...
Not Disclosed
Your CareerThe Global Regulatory and ESG Compliance Manager will drive ESG programs within the supply chain focusing on human rights environmental standards and sustainable practices. This role includes staying current with global regulations conducting gap assessments and ensuring co More...
Not Disclosed
Your CareerThe Global Regulatory and ESG Compliance Manager will drive ESG programs within the supply chain focusing on human rights environmental standards and sustainable practices. This role includes staying current with global regulations conducting gap assessments and ensuring co More...
Not Disclosed
Your CareerThe Global Regulatory and ESG Compliance Manager will drive ESG programs within the supply chain focusing on human rights environmental standards and sustainable practices. This role includes staying current with global regulations conducting gap assessments and ensuring co More...
The Medical Director Clinical Science is responsible for Sobis clinical development activities on a product/indication and serves as scientific and medical expert on matters relating to the assigned development program including operational regulatory and drug safety. Previous e More...
The Medical Director Clinical Science is responsible for Sobis clinical development activities on a product/indication and serves as scientific and medical expert on matters relating to the assigned development program including operational regulatory and drug safety. Previous e More...
The Medical Director Clinical Science is responsible for Sobis clinical development activities on a product/indication and serves as scientific and medical expert on matters relating to the assigned development program including operational regulatory and drug safety. Previous e More...
The Medical Director Clinical Science is responsible for Sobis clinical development activities on a product/indication and serves as scientific and medical expert on matters relating to the assigned development program including operational regulatory and drug safety. Previous e More...
5-7 years Our client a global pharmaceutical company is seeking a clinical systems validation manager to set strategy and policies and oversight of the Validation Department and programs of related activities.This will be a 1 year contractual position with the likelihood of renewal.Job Descript More...
destinationone Consulting specializes in recruitment across diverse sectors including CleanTech Education and EdTech Government (Municipal State/Provincial and Federal) Health and MedTech Healthcare and Wellness Legal NotForProfit and Public Accounting. We are committed to building a More...
As a Senior CRA you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigato More...
The TA Lead Global Rheumatology Pipeline leads a team in a therapeutic area in developing and executing the Medical Affairs strategy for an AbbVie asset in development or a market product. Responsible for practical and clinically meaningful data strategy and delivery to inf More...
The TA Lead Global Rheumatology Pipeline leads a team in a therapeutic area in developing and executing the Medical Affairs strategy for an AbbVie asset in development or a market product. Responsible for practical and clinically meaningful data strategy and delivery to inf More...
The TA Lead Global Rheumatology Pipeline leads a team in a therapeutic area in developing and executing the Medical Affairs strategy for an AbbVie asset in development or a market product. Responsible for practical and clinically meaningful data strategy and delivery to inf More...
The TA Lead Global Rheumatology Pipeline leads a team in a therapeutic area in developing and executing the Medical Affairs strategy for an AbbVie asset in development or a market product. Responsible for practical and clinically meaningful data strategy and delivery to inf More...
The TA Lead Global Rheumatology Pipeline leads a team in a therapeutic area in developing and executing the Medical Affairs strategy for an AbbVie asset in development or a market product. Responsible for practical and clinically meaningful data strategy and delivery to inf More...
The TA Lead Global Rheumatology Pipeline leads a team in a therapeutic area in developing and executing the Medical Affairs strategy for an AbbVie asset in development or a market product. Responsible for practical and clinically meaningful data strategy and delivery to inf More...
Our client a world leader in diagnostics and life sciences is looking for a Lab Supervisor.Duration: Long Term Contract (Possibility Of Further Extension)Responsibilities: Generates or modifies Development Laboratory Management related processes (e.g. Guidance Documents SOPs). Deve More...
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