Instagram
youtube
Facebook

Senior Director Clinical Development - Psychiatry

3+ years
Not Disclosed
10 Jan. 31, 2025
Job Description
Job Type: Full Time Education: MD Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

📌 Senior Director Clinical Development - Psychiatry | Parsippany, NJ, USA
📍 Location: Parsippany, NJ, United States
💼 Company: Teva Pharmaceuticals
🕒 Experience: 3+ years in clinical development

About Teva Pharmaceuticals

Teva Pharmaceuticals is committed to making healthcare more affordable and accessible globally. With operations in nearly 60 countries, Teva serves 200 million+ people worldwide daily. They manufacture generics and key medications on the World Health Organization’s Essential Medicines List.

Role Overview

Teva is looking for a Senior Director of Clinical Development to lead and execute clinical development programs in psychiatry. This role involves overseeing global clinical trials, providing strategic leadership, and collaborating with various functional teams. The Senior Director will also play a critical role in regulatory filings (INDs, NDAs, BLAs) and liaising with regulatory authorities.

Key Responsibilities

Leadership: Lead clinical development programs, ensuring alignment with corporate goals.
Clinical Oversight: Oversee study design, initiation, implementation, and completion of global clinical trials.
Regulatory Expertise: Lead interactions with regulatory authorities and oversee global regulatory filings.
Collaboration: Work cross-functionally with teams in medical affairs, health economics, regulatory, commercial, and supply chain.
Documentation: Oversee the preparation of clinical documents such as Clinical Study Reports, Protocols, and Investigator’s Brochures.
Strategic Partnerships: Foster relationships with key opinion leaders, academic institutions, and external collaborators.
Mentorship: Lead, mentor, and develop clinical development teams.

Qualifications

🎓 Education:

  • MD with board certification in psychiatry or relevant specialties.
  • Additional training in clinical research or drug development is a plus.

💼 Experience:

  • 3+ years in pharmaceutical/biotech industry with clinical development experience.
  • Expertise in psychiatry or related therapeutic areas.
  • Proven track record in managing programs through regulatory approvals and global clinical trials.

Desired Skills

  • Strong strategic thinking and decision-making skills.
  • Expertise in clinical trial design, data analysis, and risk management.
  • Exceptional leadership, communication, and interpersonal skills.
  • Fluent in English (oral and written).

Benefits

  • Comprehensive health insurance (medical, dental, vision).
  • Retirement savings with 401(k) match.
  • Paid time off including vacation, sick days, and holidays.
  • Life and disability protection, and additional perks like tuition assistance, paid parental leave, and more.

Work Environment

Hybrid role (3 days a week in Parsippany, NJ or West Chester, PA office, or remote for the right candidate).

📩 Apply Now

\