Pharmaceutical Clinical Director:
GPAC

884761281
GPAC
Santa Clara California
Pharmacy
Apply
Description

gpac Pharmaceutical Division: Clinical Director

Are you passionate about bringing life-changing medicines to market?

My client compoany is seeking a clinical director committed to transform the lives of patients and is a pioneer in science. They are seeking a clinical director that supports the mission and will lead a team which challenges each other to achieve excellence. They are seeking a director who will work with passion, integrity and respect. If you desire a culture of rigorous work and serious fun, you should read further.

SUMMARY

* Providing leadership and management within CD to provide scientific and clinical development support for products within assigned therapy area(s).

* Support development and execution of medical & clinical strategy for assigned product(s).

* Preparation of clinical output summary reports, Power Point presentations of the clinical data, clinical trial synopses, patient profiles

* Preparation of targeted reviews/profile of outliers, search and summarize information relevant for various clinical documents preparation

* Leading the interpretation of trial data and development and review of clinical study documents, reports etc,

* Provide relevant expertise to internal teams, including clinical operations, medical writing, data management, pharmacovigilance to ensure quality processes and deliverables.

* Address medical questions or clarify issues arising during conduct of the study

* Participation/contribution to cross-functional team meetings; Interact with external scientific leaders and/or Regulatory authorities.

* Assists Business Development with assessments and intelligence on potential new products and assists with due diligence activities as required.

* Review, analysis and report clinical trial data

* Medical review of clinical trial data.

* Serve as a scientific resource to cross-functional internal teams to facilitate quality of study execution and problem resolution.

Success Factors:

* Excellent written and oral presentation skills

* Strong critical thinking

* Ability to work effectively with cross-functional teams in a matrix environment

* Thrives in a dynamic, start-up environment

Education and Skills Requirements:

* MD required, subspecialty training is preferred

* 3-5 years of hands on pharmaceutical or biotech experience in clinical development.

* In depth knowledge of drug development process and oversight of clinical trials

* Working knowledge of biostatistics, regulatory, clinical pharmacology and pharmacokinetics

* Excellent interpersonal, written, verbal and visual communication skills

* Proven ability to successfully manage multiple tasks and prioritize accordingly

* Professional and pleasant demeanor

* Willingness to travel

Core Values of Company:

* Commitment to People

* Innovation and Discovery

* Sense of Urgency

* Open Culture

* Passion for Excellence

Compensation:

* Competitive compensation structure

* 401K

* Profit sharing

* Full medical benefits

* PTO and Vacation



If you are seeking a life-changing opportunity, apply today.

To connect with this, and other opportunities within the Pharmaceutical industry, apply with a CV/Resume to

All qualified applicants will receive consideration without regard to race, age, color, sex (including pregnancy), religion, national origin, disability, sexual orientation, gender identity, marital status, military status, genetic information, or any other status protected by applicable laws or regulations.

GPAC (Growing People and Companies) is an award-winning search firm specializing in placing quality professionals within multiple industries across the United States for the past 30 years. We are extremely competitive, client-focused and realize that our value is in our ability to deliver the right solutions at the right time.



Job Requirements:
SUMMARY • Providing leadership and management within CD to provide scientific and clinical development support for products within assigned therapy area(s). • Support development and execution of medical & clinical strategy for assigned product(s). • Preparation of clinical output summary reports, Power Point presentations of the clinical data, clinical trial synopses, patient profiles • Preparation of targeted reviews/profile of outliers, search and summarize information relevant for various clinical documents preparation • Leading the interpretation of trial data and development and review of clinical study documents, reports etc, • Provide relevant expertise to internal teams, including clinical operations, medical writing, data management, pharmacovigilance to ensure quality processes and deliverables. • Address medical questions or clarify issues arising during conduct of the study • Participation/contribution to cross-functional team meetings; Interact with external scientific leaders and/or Regulatory authorities. • Assists Business Development with assessments and intelligence on potential new products and assists with due diligence activities as required. • Review, analysis and report clinical trial data • Medical review of clinical trial data. • Serve as a scientific resource to cross-functional internal teams to facilitate quality of study execution and problem resolution.
Basic Qualifications
Requirement