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Job description
Why Us?
At Par Health, we believe great healthcare is built on getting the essentials right. We’re looking for passionate, talented individuals who share our commitment to improving lives. With a global workforce, we lead with pride and purpose—prioritizing quality and safety while fostering a culture of continuous improvement, accountability, and teamwork. Elevating the Essentials isn’t just our tagline, it’s the higher standard we live by every day.
Job Description Summary
The Global Medical Information Lead provides oversight and management of all activities pertaining to medical information inquiries for products marketed by Par Health (The Company) to ensure safe product usage and a regulatory compliant work environment. Responsible for providing technical and clinical information regarding product usage and performance. Clinically educate other members of the post-market surveillance team, call center and medical information vendor personnel, and other personnel within The Company as needed. Provide support and review of The Company’s medical and promotional material. Serve as the Business owner for the call center and medical information vendor/CRO to ensure compliant medical information globally.
ESSENTIAL FUNCTIONS
Leadership of the medical information team
Responsible for the compliance and trending of medical information inquiries with company procedures
Composes and maintains standardized response letters (SRLs); serves as the business owner for SRLs
Performs continual independent review of medical/scientific literature on The Company’s products and competitor's pharmaceutical products
Critically evaluates medical/scientific literature and determine appropriate usage
Provide support for medical review of The Company’s medical and promotional materials
Participates on cross-functional teams concerned with development or support of products as needed
Provides professional consultation in matters related to safety, efficacy, and proper product usage as needed
Provides support for Pharmacovigilance and Product Monitoring (i.e. Health Hazard Evaluations, customer letters) as needed
Serves as a member of the Signal Action Committee which performs medical and scientific review of safety signals that have been identified by the Pharmacovigilance department.
Complies with all relevant related guidelines, standards and regulations pertaining to medical information provided to customers globally
Maintains Standard Operating Procedures (SOP’s) for responding to unsolicited requests for medical information globally
Collaboratively and effectively communicates with various departments, including Legal, Regulatory Affairs, R&D, Engineering, Business Development Leadership, Commercial, Pharmacovigilance, and Customer Service.
Provide guidance to the call center and medical information vendor/CRO regarding the provision of medical information for The Company’s products globally, including ensuring the vendor has the most recent product labeling for each country. Monitor the vendor/CRO’s performance and adherence to company policies and procedures.
Performs internal quality assessments and medical review of information provided by The Company’s personnel.
Acts as the subject matter expert for medical information during audits and regulatory inspections. Participate in the drafting of audit and inspection responses and assist in the coordination and completion of corrective actions related to audits and inspections.
Prepare and deliver accurate medical information and other post-market reports on regular and ad-hoc basis and identify potential performance issues and alert appropriate management personnel when needed.
Identify, hire, train, develop and manage medical information specialists.
MINIMUM REQUIREMENTS
Advanced degree in relevant medical specialty required (i.e. PharmD, RPh, Physician’s Assistant (PA), etc.)
Experience
A minimum of five years of clinical/practical experience in a relevant clinical environment or related Post-Market Surveillance experience in the pharmaceutical and/or medical device industry.
Preferred Skills/Qualifications
Healthcare certification
Previous Medical Affairs, Regulatory Affairs, and or Medical Communications experience in the pharmaceutical industry
Experience interacting with regulatory agencies such as the FDA.
Writing skills necessary to effectively communicate technical/clinical information to others.
Skills/Competencies
Flexible leader
Highly self-motivated
Strong Communication and Presentation skills
Problem Solving and Scientific evaluation skills
Other Skills/Competencies
Sound organizational skills with the ability to prioritize tasks
Ability to build productive relationships with personnel within and outside of the department and company
Demonstrated ability to manage complex processes and cross-functional teams
Organizational Relationships/Scope
Reports to the Product Monitoring and Medical Information Lead
Manages a team that includes professional individual contributors
Interact with a variety of departments and locations. These include, but are not limited to, Legal, Regulatory Affairs, Product Monitoring, Pharmacovigilance, R&D, Marketing, Quality Assurance, Sales, and Customer Service. The degree and scope will vary according to the needs of the departments involved
Working Conditions
Normal office conditions, which include sitting for long periods of time and computer and phone use.
Occasional travel may be required for such things as training seminars, manufacturing site visits, and professional/trade conventions.
Disclaimer
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position.
EEO Statement
We comply with all applicable federal, state, and local laws prohibiting discrimination and harassment, and provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status, or genetic information, or any other classification protected by federal, state or local law. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.
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Worksite address
woodcliff lake, NJ, 07677, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.