Vice President, Reproductive Medicine

Ferring Pharmaceuticals•Parsippany, NJ

About The Position

At Ferring Pharmaceuticals, we help people around the world build families and live better lives. We are entrepreneurial and innovative, with a global team focused on scientific advances in the areas of reproductive and women’s health, gastroenterology and urology. Ferring + You is all about working together and sharing ideas, so that we can bring science to life for patients around the world. Joining our R&D teams, you will discover an empowering culture and the opportunity to create and deliver innovative products that have the potential to change lives. Collaborating with colleagues inside and outside Ferring, we are focused on growing our capabilities with new therapeutics, life-cycle management and personalised solutions. Doing revolutionary work is in your hands. Ferring+You As VP of Reproductive Medicine, you will strengthen and build the future of our Reproductive Medicine portfolio by driving innovation in clinical development and evidence generation, while serving as a trusted medical and scientific advisor for global project teams and government regulatory agencies. Reporting directly to the Chief Medical Officer, your leadership will be instrumental in strategy development for the therapeutic area. The successful candidate will have the opportunity to build an organization which leverages the agility of a mid-size company with the unique global footprint of Ferring. Your day at Ferring Your primary responsibilities include: Designing and overseeing the direction, planning, execution, monitoring, interpretation and reporting of clinical research programs from phases I– IV inclusive, including clinical trials, real world evidence studies and other evidence generation activities relating to studies of humans. Building relationships with key opinion leaders and applies their input to enhance study design and protocols. Assuring that clinical research program design meets scientific objectives and is aligned with commercial needs. Serving as medical/scientific consultant to global brand or global project teams and government regulatory agencies. Establishing the criterion essential for determining the safety, efficacy, and medical utility of products in development or marketed products. Supporting the reporting of information submitted to the regulatory agencies for new drug or medical device applications and to sustain marketing authorizations, including label updates. Participating in and coordinating adverse event reporting and safety responsibilities monitoring, signing off on product safety reviews. Behind our innovation…There’s you A Doctor of Medicine (M.D.) degree is required, preferably with a specialization in gynecology and obstetrics, or endocrinology. In addition to solid expertise as a clinician, the candidate must have strong pharmaceutical industry experience, preferably from a medical and/or clinical and/or pharmacovigilance organization. Strong stakeholder management skills, as well as ability to navigate organizational complexity and ambiguity. Experience managing a team in a matrix organization is an asset. Strategic mindset, forward looking. Exceptional communication and influencing skills. Able to adapt communication style to all levels. People come first at Ferring Get inspired from our commitment to advocate for everyone’s right to build a family, no matter who you are, where you live or who you love Our inclusive support package – “Building Families at Ferring” provides equal and accessible policies for all employees who wish to start their family journey, ensuring a global standard, irrespective of location and role. Subject to a minimum period of employment at Ferring. Parental leave for both birthing and non-birthing parents Extended support on family building journey Making a difference in the life of millions of people means we succeed by working together. Our diverse backgrounds, experiences, expertise, and perspectives enable us to find solutions to even the most challenging problems, and our success is tied to each team member’s contributions. Imagine the power of your career when it’s Ferring + You. Behind our purpose… There’s you If our mission and your vision are aligned, please apply! We strive to build and maintain an inclusive and diverse workplace with equal opportunities and mutual respect for all employees regardless of their backgrounds and socioeconomic status. Note to agencies: this search is being managed by Ferring’s Talent Acquisition team. Kindly do not send us spontaneous profiles. Location: Ferring UK Ferring Pharmaceuticals a privately owned, research-driven, specialty biopharmaceutical group committed to building families and helping people live better lives. We are leaders in reproductive medicine with a strong heritage in gastroenterology and urology, and are at the forefront of innovation in uro-oncology gene therapy. Ferring was founded in 1950 and employs more than 7,000 people worldwide. The company is headquartered in Saint-Prex, Switzerland, and has operating subsidiaries in more than 50 countries which market its medicines in over 100 countries. Learn more at www.ferring.com, or connect with us on LinkedIn, Instagram, YouTube, Facebook and X. At Ferring, we'll give you the tools to shape a career build on purpose. Join us and help People around the world to build families and live better lives. Click HERE to enlarge the picture. At Ferring, our focus on Patient Advocacy drives our commitment to create more equitable health outcomes for all, at every stage of their healthcare journey. We believe in everyone’s right to access the best treatment, pioneering into new therapeutic areas, and developing innovative ways to diagnose, treat and prevent diseases. Don't see the dream job you are looking for? Drop off your contact information and resume and we will reach out to you if we find the perfect fit!

Requirements

A Doctor of Medicine (M.D.) degree is required, preferably with a specialization in gynecology and obstetrics, or endocrinology.
In addition to solid expertise as a clinician, the candidate must have strong pharmaceutical industry experience, preferably from a medical and/or clinical and/or pharmacovigilance organization.
Strong stakeholder management skills, as well as ability to navigate organizational complexity and ambiguity.
Strategic mindset, forward looking.
Exceptional communication and influencing skills.
Able to adapt communication style to all levels.

Nice To Haves

Experience managing a team in a matrix organization is an asset.

Responsibilities

Designing and overseeing the direction, planning, execution, monitoring, interpretation and reporting of clinical research programs from phases I– IV inclusive, including clinical trials, real world evidence studies and other evidence generation activities relating to studies of humans.
Building relationships with key opinion leaders and applies their input to enhance study design and protocols.
Assuring that clinical research program design meets scientific objectives and is aligned with commercial needs.
Serving as medical/scientific consultant to global brand or global project teams and government regulatory agencies.
Establishing the criterion essential for determining the safety, efficacy, and medical utility of products in development or marketed products.
Supporting the reporting of information submitted to the regulatory agencies for new drug or medical device applications and to sustain marketing authorizations, including label updates.
Participating in and coordinating adverse event reporting and safety responsibilities monitoring, signing off on product safety reviews.

Benefits

Our inclusive support package – “Building Families at Ferring” provides equal and accessible policies for all employees who wish to start their family journey, ensuring a global standard, irrespective of location and role.
Parental leave for both birthing and non-birthing parents
Extended support on family building journey

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