Bayer Global Regulatory Affairs Regional Regulatory Manager in Whippany, New Jersey

Your tasks and responsibilities

The primary responsibilities of this position, Global Regulatory Affairs Regional Regulatory Manager, are to: •The Global Regulatory Affairs Regional Regulatory Manager will be functioning within a Therapeutic Area structure. The scope of the Regional Regulatory Manager position includes the preparation, coordination, and strategic presentation of Regulatory documents to local Health Authorities (HA) for registration and maintenance of new and existing products in the U.S. or EU. The position is responsible for contributing to the development of regulatory strategy, tactics, and direction to new product development in preparation of submission documents, responses to queries by regulatory authorities and setting and developing processes to improve performance, perpetually meeting the changing regulatory environment •Acts as an interface between Bayer and the local Health Authority (HA). Organizes and drives preparations for meetings and teleconferences with HA officials to discuss compliance matters or issues that may arise during the development of a new product. Drives development, completion, and submission to HA of any materials required for such meetings. •Submits regulatory information to the HA. Reviews HA submissions to assure compliance with HA regulations. Reviews and determines the applicability of supporting documentation for inclusion in regulatory submissions for accuracy, completeness, and scientific consistency. •Works closely with the GRS for the assigned product/project, as well as Global Clinical, Medical Affairs, Drug Safety, Quality Assurance, and other functions to monitor product related corporate activities for regulatory compliance, including all manufacturing, preclinical and clinical plans and practices. Provides guidance to other functions / staff to assure that clinical trial programs are carried out in accordance with all regulations and Bayer Standard Operating Procedures, so that data from these trials can be used to prepare high quality, approvable submissions and that Bayer or an investigator can withstand HA inspection. •Participates in the Global Regulatory Team to provide input for all phases of drug development for investigational products and/or licensed projects, contributing to the development and implementation of the Global Regulatory Plan, particularly with regard to addressing local HA requirements and the needs of the local market. •Provides local region-specific input to the GRS for discussion at Global Project Teams for a particular investigational or licensed product. Participates in ad hoc Global Project Team sub-teams or working groups as invited by the Global Project Team. •Interacts with responsible departments and functions to provide input to the GRS in support of the collection, review, and assembling of the scientific (preclinical, clinical, and manufacturing) and administrative sections of submissions to regulatory agencies for a particular investigational or licensed product. •Interacts with Company Partners (including marketing partners and contract manufacturers) and Consultants for various regulatory matters as needed. •Responsible for creating and/or managing a strong network for assigned projects with the health authority in the assigned region, and other key regulatory influencers and stakeholders, that facilitates the incorporation of regulatory intelligence and influence into the regulatory project strategy with the goal to increase overall approval chances. •Where applicable, reviews promotional materials on global level (Interface to promotional integration team).

Who you are

Your success will be driven by your demonstration of our LIFE values. More specifically related to this position, Bayer seeks an incumbent who possesses the following: •Advanced technical degree (Ph.D., M.D., D.V.M. or Pharm.D.) in life sciences, OR technical degree (B.Sc. or M.Sc.) with at least 1 year of prior regulatory experience. •Good communication skills, verbal and written, are imperative. •The ability to work within a global team framework and a multicultural environment is required. •Strong analytical skills are necessary to interpret regulatory data and make critical decisions. •Supervision: Manages and coordinates regulatory projects, works independently with moderately high supervision.

Preferred Qualifications: •Familiarity with local Health Authority (HA) regulations (FDA or EMA), especially as they apply to preclinical and clinical disciplines to support filings, is desirable. It is also desirable that the individual have knowledge of medical procedures, drug therapy, statistical concepts, and the collection, computerization and reporting of data collected in clinical trials.

Your application

Bayer offers a wide variety of competitive compensation and benefits programs. If you meet the requirements of this unique opportunity, and you have the "Passion to Innovate" and the "Power to Change", we encourage you to apply now. Job postings will remain open for a minimum of ten business days and are subject to immediate closure thereafter without additional notice. To all recruitment agencies: Bayer does not accept unsolicited third party resumes.

Bayer is an Equal Opportunity Employer Minorities / Females / Protected Veterans / Disabled

Country:United States


Reference Code:0000178147