Associate Director, Regulatory Operations - Boston, MA

The Clinical and Translational Investigation Program (CTIP) was established in 2010 to centralize and standardize conduct of clinical research within the Dana-Farber/Boston Children's Cancer and Blood Disorders Center.The Regulatory Operations Manager will oversee the CTIP Regula ...

+The OpportunityIf you're energized by solving complex problems, digging into details, and playing a direct role in protecting a firm from financial and regulatory risk, this is the role for you. · ...

The Clinical and Translational Investigation Program (CTIP) was established in 2010 to centralize and standardize conduct of clinical research within the Dana-Farber/Boston Children's Cancer and Blood Disorders Center. · The Regulatory Operations Manager will oversee the CTIP Reg ...

The Clinical and Translational Investigation Program (CTIP) was established in 2010 to centralize and standardize conduct of clinical research within the Dana-Farber/Boston Children's Cancer and Blood Disorders Center.CTIP Regulatory unit will provide pan-CTIP support as part of ...

The OpportunityAs a Regulatory Operations Consultant you will be responsible for mitigating risk for the firm by evaluating exception reporting to ensure adherence to the firm's supervisory controls as well as state, FINRA, and SEC rules and regulations. · ...

The Clinical and Translational Investigation Program (CTIP) was established in 2010 to centralize and standardize conduct of clinical research within the Dana-Farber/Boston Children's Cancer and Blood Disorders Center. · Meet regularly with the leadership / key stakeholders to id ...

Our client is seeking an experienced Regulatory Operations Consultant to support Veeva Vault RIM. · ...

We are seeking an experienced Regulatory Operations Consultant to support Veeva Vault RIM. · This role will play a key part in submission readiness. · ...

The Associate Director of Regulatory Operations is responsible for assisting the Head of Regulatory Operations in maintaining Rhythm's regulatory submission standards and current electronic submission guidelines/requirements. · The role involves managing the preparation of eCTD s ...

+ Job summary: The Associate Director of Regulatory Operations is responsible for maintaining Rhythm's regulatory submission standards. + Responsibilities: Manage regulatory operations activities; prepare eCTD submission-ready documents; collaborate with cross-functional teams. + ...

The Associate Director Regulatory Operations role will be responsible for daily operational activities within Regulatory Affairs to ensure delivery of timely accurate and high-quality submissions to regulatory health authorities. · Responsible for forward planning of publishing r ...

The Associate Director of Regulatory Operations is responsible for assisting the Head of Regulatory Operations in maintaining Rhythm's regulatory submission standards and current electronic submission guidelines/requirements. This role involves managing the preparation of eCTD su ...

+Job summary+Company Overview · Rhythm is a global commercial-stage biopharmaceutical company committed to transforming the lives of patients and their families living with rare neuroendocrine diseases.+ · +Responsibilities And Duties+Manage regulatory operations activities ensur ...

+The Associate Director, Regulatory Operations role will be responsible for daily operational activities within Regulatory Affairs to ensure delivery of timely, accurate and high-quality submissions to regulatory health authorities. · +Responsible for forward planning of publishi ...

We're hiring a Senior Analyst, Regulatory Operations to join our Regulatory team. · ...

The Sr.Regulatory Analyst is an important member of the Regulatory Operations team responsible for project managing and supporting discrete tasks to ensure Oscar is compliant with federal and state product filing requirements. · Manage the preparation and filing of Oscar's commer ...

We re hiring a Senior Analyst Regulatory Operations to join our Regulatory team. · The Sr. Regulatory Analyst is an important member of the Regulatory Operations team responsible for project managing and supporting discrete tasks to ensure Oscar is compliant with federal and stat ...

The Associate Director of Regulatory Operations will lead strategy, infrastructure, and execution for all regulatory submissions (INDs, CTAs, NDAs), ensuring timely, compliant filings with health authorities (FDA, EMA, · APAC HAs) by managing teams, · processesystems(eCTD)and cro ...

The Associate Director Regulatory Operations will be responsible for submission management across the development pipeline and support the commercial portfolio. · This hands-on position will also assist with regulatory affairs systems applications and tools including supporting s ...

The Executive Director of Global Regulatory Operations leads teams responsible for publishing submissions management regulatory information management compliance. · This role will be accountable for creating high quality organization utilizing best technology process project mana ...