Clinical Development Director - Psychiatry

3+ years

Not Disclosed

West Chester

10 Jan. 3, 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

Clinical Development Director - Psychiatry
Location: West Chester, PA, USA
Date Posted: January 3, 2025

Join Teva Pharmaceuticals, a global leader committed to making healthcare accessible and affordable worldwide. As part of our diverse team spanning nearly 60 countries, you’ll help improve the lives of millions daily by delivering innovative treatments and essential medicines.

The Opportunity

The Clinical Development Director will spearhead clinical programs worldwide, overseeing all phases of clinical research for psychiatry-related products. You will lead cross-functional teams in a matrix environment and manage clinical development plans while ensuring compliance with regulatory requirements and company objectives.

Key Responsibilities

Strategic Leadership:
- Serve as a core member of the Global Program Team.
- Develop and manage comprehensive Clinical Development Plans.
Clinical Operations:
- Support trial initiation, resource planning, and study execution.
- Provide clinical leadership in protocol development and study design.
Regulatory and Safety Oversight:
- Represent clinical development in Health Authority meetings globally.
- Act as the medical monitor to guide investigator selection, patient safety, and study conduct.
Stakeholder Engagement:
- Build and maintain partnerships with internal teams and external stakeholders, including Key Opinion Leaders (KOLs).
- Present at investigator meetings and relevant venues.
Documentation and Reporting:
- Prepare protocols, Investigator’s Brochures, Clinical Study Reports, and regulatory submissions.

Your Qualifications

Education:
- MD required.
- Board certification or strong clinical development experience in psychiatry.
Experience:
- Minimum 3 years in pharmaceutical industry clinical development.
- Proven ability to lead studies from early phases to regulatory submission.
Skills:
- Strong leadership and interpersonal skills.
- Exceptional oral and written communication skills.
- Fluent in English.

Work Environment

This hybrid role is based on-site 3 days a week in either West Chester, PA or Parsippany, NJ.

Benefits

Health & Wellness:
- Comprehensive Medical, Dental, Vision, and Prescription coverage starting on Day 1.
Financial Security:
- 401(k) with employer match up to 6%, plus an annual 3.75% Defined Contribution.
Work-Life Balance:
- Generous Paid Time Off (vacation, sick leave, holidays) and parental leave.
Additional Perks:
- Employee Assistance Program, Stock Purchase Plan, Tuition Assistance, and more.

Equal Employment Opportunity

Teva Pharmaceuticals is committed to creating an inclusive workplace. Employment opportunities are available to all, regardless of age, race, creed, religion, disability, gender identity, veteran status, or any legally protected category.

Application Process for Current Teva Employees
Employees are encouraged to apply through the internal Employee Central portal for priority consideration.

Notice to Employment Agencies
Teva Pharmaceuticals does not accept unsolicited assistance from agencies without prior written agreements.

Start your journey with Teva today and make a meaningful impact on global health!

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Clinical Development Director - Psychiatry

Job Description

The Opportunity

Key Responsibilities

Your Qualifications

Work Environment

Benefits

Equal Employment Opportunity

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