Medical Director, Clinical Operations - Medical Affairs
Becton, Dickinson and Company
August 8, 2018
Franklin Lakes, New Jersey
Full Time - Experienced
Medical Director, Clinical Operations - Medical Affairs
Franklin Lakes, NJ* Job ID – R-314793
BD is a leading global medical technology company that creates medical technology, devices and laboratory equipment for a variety of needs across the healthcare continuum. At BD, we are looking for candidates who possess passion, innovative solutions and a commitment to our one mission of improving access to groundbreaking medical and biotechnology services for people near and far, delivering state-of-the-art technology and cutting-edge research in the battle to fight and cure infectious diseases. With global reach that extends across 50 countries worldwide, our network of professionals collaborates on effective measures to deliver enhanced patient quality such as lower health care delivery costs, improved health care and safety, and expanded health care for all.
Reporting to the WW Vice President, Medical Affairs (MA), BD Diagnostics - Preanalytical Systems, this position is leading the PAS MA Laboratory Operations and is member of the World-Wide PAS MA Leadership Team and the Global Clinical Council (GCC) Core Team.
This position has the responsibility to provide medical, scientific, technical, and laboratory customer-focused leadership and perspective, and is responsible for clinical study execution for Clinical studies supporting all aspects of FDA requirements throughout the BD PAS product life cycle (new product development, sustaining engineering and post-market), data analysis and review, as well as for scientific integrity. This position is also responsible for executing the clinical study portfolio to support FDA regulations by working closely with regulatory. Directly reporting to this position is the Clinical Laboratory Manager, MA Manager - FDA Projects.
Operations of the PAS MA Laboratory Operations group, including but not limited to: people management, budgeting, and resource allocation.
Reviewing of clinical study synopsis and protocols. Managing clinical studies conducted in PAS MA Clinical Laboratory and outside locations for PAS.
Working closely with PAS MA Leadership Team in the preparation of response to FDA and ensure that all agreed timelines and deliverables are met.
Providing medical expertise for timely completion of Situation Analysis, Health Hazard Evaluations and NCMRS.
Being a part of PAS MA Leadership Team.
Supporting FDA related priorities such as clinical studies and risk assessment.
As part of the PAS MA LT contributes to the development of the PAS MA strategy.
Operations of the PAS MA Laboratory and timely completion of Situation Analysis, Health Hazard Evaluations and NCMRS.
Sphere of Influence:
Playing an important role in influencing key business decisions within PAS MA. Serves on the world-wide PAS Medical Affairs leadership team and the Global Clinical Council Core Team.
Playing an important role in resource planning within PAS MA by managing resourcing of internal clinical trials PAS MA Laboratory Operations.
Clinical Laboratory Manager, MA Manager- FDA Projects.
PAS MA Leadership Team, GCC Core Team
Core Team Leaders, PAS Regional MA leaders, Regulatory and Quality.
KOLs in Laboratory Medicine.
Reviewing clinical study design for clinical studies throughout the BD PAS product life cycle (new product development, sustaining engineering and post-market), data analysis and review.
Ensuring the safety and efficacy of all products and services offered by PAS. Will conduct all health risk assessments within PAS and recommend field actions in case of product issues.
If applicable, impact on quality: Works with Quality and Regulatory Compliance to assess impact of product issues on patient’s health.
The key financial impact of this position is on the timely delivery on new products on the market and ability to meet planned growth targets. Also, through the accountability of safety and efficacy of all BD PAS products, this role has the impact on execution of projected sales targets through assessment of potential product deficiencies and need to remove affected product from the market.
Managing the budgets of internal PAS clinical trials and for PAS MA Laboratory Operations.
KSA Requirements (Knowledge, Skills, and Abilities)
University degree in medicine (MD) and specialty training in clinical pathology.
Certifications a plus.
License to practice medicine is a plus.
Experience in the field of laboratory medicine/pathology is required.
Experience in a medical device/IVD company is a plus.
Strong knowledge of Laboratory Medicine.
Knowledge of a scientific discipline related to Clinical Pathology.
Strong knowledge of clinical laboratory operations.
Knowledge of the preanalytical phase of the total testing process is a plus
Excellent interpersonal skills.
Demonstrated leadership skills.
Demonstrated strong customer/client orientation
Demonstrated capability for strategic thinking, excellent analytical and problem solving skills.
Ability to work with teams and to provide leadership within the medical community
Ability to integrate medical, scientific, and technical information and effectively communicate these data to the scientific community, customers, as well as throughout the organization.
Ability to network/develop relationships with KOLs
Project management skills
Strong competency in the areas of clinical study design, statistics, technical writing.
Demonstrated ability to understand, interpret and explain complex clinical and scientific information.
Strong communication skills (verbal, presentation, written).
We offer a competitive salary and comprehensive benefits package. For immediate consideration, please apply online at: