Teva Pharmaceuticals Senior Medical Director -Clinical Development Headache in Frazer, Pennsylvania

Senior Medical Director -Clinical Development Headache

Date: Dec 7, 2018

Location: Frazer, Pennsylvania, US, 19355

Company: Teva Pharmaceutical Industries Ltd.

Company Info

Teva is a global pharmaceutical leader and the world’s largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world’s largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we’ve built a promising pipeline centered around our core therapeutic areas. We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!

Job Description

Will be a core member of the Global Project Team

Will have and maintain the expertise necessary for the clinical development of the product

Prepares and manages multiple Clinical Development Plans

Leads or oversees the cross-functional clinical development team

Supports Global Clinical Operations in clinical trial initiation, resource planning, study implementation and successful completion

Leads a team of clinical study physicians also accountable for their respective clinical trials.

Makes presentations at the Investigator Meetings and other relevant internal or external Venues

Responsible for securing the required human resources to implement the Clinical Development Plan

Provides clinical leadership and expertise in meetings with Health Authorities globally.

Works with Clinical Supplies Group to ensure clinical drug supply plans and timely procurement with the clinical supplies group

Qualifications

MD, DO, PhD or equivalent combination of education and related work experience.

Pharmaceutical industry experience with 8+ years of experience developing and directing clinical trials.

Require 2-4 years managerial experience.

Board certification and/or strong experience in clinical development in designated therapeutic area(s) strongly preferred.

Board certification and medical training preferred.

Must speak fluid English and be a proficient scientific writer.

Proven track record of leading studies from early stage through to regulatory submissions.

Function

Research & Development

Sub Function

Clinical Development

Reports To

In process of validation

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.

Nearest Major Market: Philadelphia

EOE including disability/veteran