Principal Clinical Research Scientist
EMD Serono

Billerica, Massachusetts

This job has expired.


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.

Your role:

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 as well as data interpretation. You will have a major input into study designs, regulatory documents, and publications. You mayprovide scientific input into pipeline programs and support interactions with Regulatory Authorities. 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.

Minimum Qualifications:

  • Life sciences degree with a minimum of 6+years of experience in the pharmaceutical industry or healthcare setting, withadvanced degree in life sciences (e.g., PharmD, PhD, MS, MPH).
  • Educational and/or work experience in Neurology, specifically in Multiple Sclerosis, is required.
  • Clinical development experience is required.
  • Experience in leading 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, organize and lead teams and meetings.

Preferred qualifications:
  • Excellent written/verbal communication and presentation skills.
  • Advanced level of organizational and project management skills.
  • Experience interacting with development operations (clinical operations, regulatory, QA), clinical investigators and regulatory authorities.

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 athttps://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.

Job Requisition ID: 221827

Location: Billerica

Career Level: D - Professional (4-9 years)

Working time model: full-time


This job has expired.

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