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Project Manager III R&D Project/Program Management

Date: Mar 6, 2019

Location: Frazer, Pennsylvania, US, 19355

Company: Teva Pharmaceuticals

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

The Clinical Planning & Analysis Manager is responsible for implementation and execution of Teva R&D Global Specialty Development, "Smart Planning" processes. Including implementation of methodologies supporting study design concept and protocol optimization, budget simulation, recruitment supportive processes (country and site selection), and defining recruitment strategy.

CP&A Manager will be required to lead cross functional teams  including Internal Teva teams (operations, clinical development. Procurement, Finance etc.) and external suppliers/vendors (CRO, others) through clinical trial planning processes

CP&A Manager will Lead development and implementation of new planning methodologies including identifying stakeholders, defining project scope, working team and deliverables, running market research analysis for new technologies / solutions / tools, and selecting new technologies to support new methodologies

Qualifications

Bachelors or higher degree in Science, Industrial Engineering, or equivalent combination of education and related work experience.

At leaset 4-5 years' experience as a project manager in Clinical trial planning/feasibility departments, study start up team, study manager or equivalent in other sponsors, CRO or relevant vendors. Ability to effectively interact with and influence others without direct reporting relationships

Experience in setting new methodologies and processes in clinical trials related organizations, ICH-GCP

Functional Knowledge: proven knowledge in clinical studies and clinical development processes

Competencies: Strong resources management and project management skills, Critical thinking and analytical and problem solving skills, Interpersonal and communication skills, Ability to work as a part of a global team and independently, Strong organizational skills with ability to manage multiple project initiatives simultaneously, Strong technology orientation

Function

Project Management

Sub Function

RandD

Reports To

Michal Gueron, Associate Director, Smart Planning & CRIM

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

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