Associate Director, Clinical Safety MD

Daiichi Sankyo
Basking Ridge, New Jersey, United States
Full-time

Join a Legacy of Innovation 110 Years and Counting!

Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and technology.

With more than 120 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and its 16,000 employees around the world draw upon a rich legacy of innovation and a robust pipeline of promising new medicines to help people.

In addition to a strong portfolio of medicines for cardiovascular diseases, under the Group’s 2025 Vision to become a Global Pharma Innovator with Competitive Advantage in Oncology, Daiichi Sankyo is primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders.

Summary

This position supports safety monitoring and risk management activities, provides insights on current clinical practice and guidelines, reviews and provides written assessments of relevant medical topics, and supports PV Operations' medical review function.

This position supports a senior physician in evaluating and mitigating safety signals as they arise. Additionally, this position works with other CSPV staff and cross functional Safety Management Team (SMT) members, often handling straight-forward CSPV tasks such as single event level AE causality assessment.

This position requires manager review and gains industry knowledge through multiple opportunities.

Responsibilities

  • Safety Expert Overall : Develops safety knowledge working closely with CSPV management.
  • Safety Expert Signal Identification : Carries out routine signal identification activities formulated by manager. Uses medical knowledge to aid the SMT’s signal identification efforts.
  • Safety Expert Signal Evaluation : Assists manager in assessing new signals.
  • Safety Expert Risk Mitigation & Communication : Communicates any safety concerns to management and relevant team members.
  • Reports and Submissions : May contribute to writing minor safety sections of the NDA, CSR, and IB. May review any safety submissions for medical accuracy.

Qualifications : Successful candidates will be able to meet the qualifications below with or without a reasonable accommodation.

Education Qualifications (from an accredited college or university)

MD with board eligibility preferred

Experience Qualifications

1 or More Years of clinical experience preferred

Daiichi Sankyo, Inc. is an equal opportunity / affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.

30+ days ago
Related jobs
Promoted
Daiichi Sankyo
Bernards, New Jersey

The Director, Clinical Safety, will be a product safety lead or part of a product safety team, and be responsible for overall product safety strategy or specific areas of safety surveillance and risk management, and provide safety leadership including but not limited to clinical studies, post-market...

Promoted
Novartis Group Companies
East Hanover, New Jersey
Remote

The Associate Director, Clinical Education is a self-motivated and clinically trained leader who engages Health Care Providers (HCPs) on disease state awareness, clinical education, and specific clinical information pertaining to Novartis products. The Associate Director, Clinical Education is the f...

Promoted
Insmed Incorporated
Bridgewater Township, New Jersey

Director of Clinical Quality Assurance, the Associate Director of Clinical Quality Assurance (CQA) serves as a CQA lead representative on the development team assuring quality and regulatory compliance related to GCPs and other related activities performed by Medical/Clinical Departments. Establishi...

Promoted
Daiichi Sankyo
Bernards, New Jersey

Study outputs: Draft responses to IRBs and Health Authorities; Collaborates with Translational Medicine and Clinical Pharmacology to ensure appropriate biomarker, PK / PD measurements; Reviews emerging clinical data regularly; Leads dose-escalation meetings; Performs quality assessment with Delivery...

Promoted
Insmed Incorporated
Bridgewater, New Jersey

The Associate Director, Clinical Project & Planning Management is a member of the Clinical Business Operations team within Development Operations and provides oversight and leadership across clinical programs/trials in areas of project management and planning, including related systems/tools, timeli...

Regeneron Pharmaceuticals, Inc
Bernards, New Jersey

We are looking for an Associate Director, within our Clinical Pharmacology group. A day in the life an Associate Director may look like:. Provide clinical pharmacology subject matter expertise to the Clinical Study Team/ Development Team. Medicine (MD) and at least 5 years of relevant Clinical Pharm...

HireTalent
Bernards, New Jersey

Provides integrated safety input into all safety relevant parts of regulatory documents (IB, CCDS, RMP, REMS, DSUR, PSUR, SmPC, PI, CSR, Clinical Overview and Integrate safety summary) required during active development, submission phase and during marketing phase. Job Title: Director Clinical Safet...

Regeneron Pharmaceuticals, Inc
Bernards, New Jersey

The Associate Director reports to the Director, Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs. The Associate Director Clinical Sciences leads in the development, evaluation, p...

Bristol Myers Squibb
New Brunswick, New Jersey

The Associate Director, CSCL Customs & Trade Operations works in partnership with BMS Global Customs & Trade Compliance (C&TC) and closely with various other internal departments, external vendors, and government agencies to facilitate smooth and efficient import/export processes. Those aren’t words...

Regeneron Pharmaceuticals, Inc
Bernards, New Jersey

The Associate Director will work closely with the Director. The Associate Director, Program and Project Planning will be integral in driving a planning culture within the Global Development organization and ensuring data quality. This Associate Director will serve as a subject matter expert in plann...