A career with EMD Serono is an ongoing journey of discovery: our
58,000 people are shaping how the world lives, works and plays
through next generation advancements in Healthcare, Life Science
and Electronics. For more than 350 years and across the world we
have passionately pursued our curiosity to find novel and vibrant
ways of enhancing the lives of others. EMD Serono is a business of
Merck KGaA, Darmstadt, Germany.
United As One for Patients, our purpose in Healthcare is to help
create, improve and prolong lives. We develop medicines,
intelligent devices and innovative technologies in therapeutic
areas such as Oncology, Neurology and Fertility. Our teams work
together across 6 continents with passion and relentless curiosity
in order to help patients at every stage of life. Joining our
Healthcare team is becoming part of a diverse, inclusive and
flexible working culture, presenting great opportunities for
personal development and career advancement across the globe.
As a subject matter expert, you will partner with the Medical
Director to provide scientific, clinical, strategic, and
operational input to a late-stage clinical development program. You
will organize and lead data review and monitoring and contribute to
data interpretation, study designs, regulatory documents, and
publications. You may be asked to provide scientific input into
pipeline programs. In your role, you will closely collaborate with
other internal functions as well as external partners, such as
contract research organizations and medical experts.
Who You Are:
You are a strong team player with analytical skills, strategic
thinking, and a growth mindset. You can seamlessly work in a
dynamic, matrix organization, with experience in cross-functional
and international teams.
- Life sciences degree with a minimum of 4+ years of experience
in the pharmaceutical industry or healthcare setting.
- Advanced degree in life sciences (e.g., PharmD, PhD, MS, MPH)
- Educational and/or work experience in Neurology, specifically
in Multiple Sclerosis, is strongly desirable
- Experience in analysis and interpretation of clinical data and
a working knowledge of biostatistics, ICH-GCP, and regulatory
requirements for clinical studies.
- Ability to work both independently and collaboratively in a
fast-paced, team-based matrix environment
- Excellent written/verbal communication and presentation
- High level of organizational and project management skills
- Experience interacting with development operations (clinical
operations, regulatory, QA) and clinical investigators
What we offer: With us, there are always opportunities to break
new ground. We empower you to fulfil your ambitions, and our
diverse businesses offer various career moves to seek new horizons.
We trust you with responsibility early on and support you to draw
your own career map that is responsive to your aspirations and
priorities in life. Join us and bring your curiosity to life!
Curious? Apply and find more information at https://jobs.vibrantm.com
The Company is an Equal Employment Opportunity employer. No
employee or applicant for employment will be discriminated against
on the basis of race, color, religion, age, sex, sexual
orientation, national origin, ancestry, disability, military or
veteran status, genetic information, gender identity, transgender
status, marital status, or any other classification protected by
applicable federal, state, or local law. This policy of Equal
Employment Opportunity applies to all policies and programs
relating to recruitment and hiring, promotion, compensation,
benefits, discipline, termination, and all other terms and
conditions of employment. Any applicant or employee who believes
they have been discriminated against by the Company or anyone
acting on behalf of the Company must report any concerns to their
Human Resources Business Partner, Legal, or Compliance immediately.
The Company will not retaliate against any individual because they
made a good faith report of discrimination.