Sanofi

Senior Clinical Research Director - Oncology

Sanofi$236K — $393K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Medical Doctor (MD) or equivalent with training in Oncology and/or Hematology, experience in myeloma preferred.
  • At least 4 years experience in clinical development in pharmaceutical industry, CRO, or healthcare institution.
  • Excellent verbal and written communication skills in English with both internal and external stakeholders.
  • Adept at problem solving and thoughtful risk-taking with a risk-management approach.
  • Demonstrated ability to work effectively in a multi-functional team to achieve project milestones.
  • Understanding of regulatory, quality, and compliance standards with a quality-focused mindset.
  • International and intercultural working skills.

Responsibilities

  • Establish or adapt clinical development and contingency plans in collaboration with clinical investigators and regulatory authorities.
  • Author protocols, clinical sections of Investigator Brochure, IND/IMPD fillings, and annual reports.
  • Lead clinical interpretation of study results and contribute to clinical study reports.
  • Provide medical guidance to ensure optimal planning and execution of clinical trials.
  • Present clinical study results and development strategies to internal and external stakeholders.
  • Author clinical abstracts, presentations, and manuscripts for conferences.

Benefits

  • Supportive work environment promoting career development and growth opportunities.
  • Comprehensive rewards package recognizing individual contributions.
  • Wide range of health and wellbeing benefits including quality healthcare and wellness programs.
  • Generous parental leave policy with at least 14 weeks' gender-neutral leave.
  • Opportunities for promotions or lateral moves, both locally and internationally.
Full Job Description
Job Title: Clinical Research Director - Oncology

Location: Cambridge, MA, Morristown, NJ

As a Senior Clinical Research Director (Senior CRD) within the Oncology Therapeutic Area, you will lead the clinical trial strategy for one or more multiple myeloma assets, creating synergies across Clinical Operations, Biostatistics, Regulatory, Translational Medicine, Project Management, New Product Planning and Pharmacovigilance to establish the development strategy and execute the development plan.

Main Responsibilities
  • Working within a matrix model, establish or adapt clinical development and contigency plans by engaging with clinical investigators, advisors and regulatory authorities.
  • Author protocols, extended synopses, clinical sections of the Investigator Brochure, IND/IMPD fillings, annual reports, development risk management plans.
  • Lead the clinical interpretation of study results
  • Contributes to clinical study reports and clinical summaries, including regulatory submissions.
  • Provide expert medical guidance to other functions, including Clinical Operations, Biostatistics and Translational Medicine, to ensure optimal planning and execution of clinical trial
  • Present and discuss development strategy and clinical study results with key internal stakeholders, external investigators, advisory boards, and regulatory authorities
  • Author clinical abstracts, presentations for conferences, and manuscripts


About You

Education
  • Medical Doctor (MD) or equivalent; training in Oncology and/or Hematology, preferably with experience in myeloma or hematologic malignancies is a plus.

Experience
  • At least 4 years experience in clinical development in the pharmaceutical industry, CRO, or healthcare institution

Soft skills
  • Excellent communication skills (verbal and written English) with both internal and external stakeholders
  • Adept at problem solving
  • Thoughtful risk-taking: challenge decisions and status quo with a risk-management approach
  • Demonstrated ability to work with a multi-functional team to achieve project milestones.
  • Understanding of and willingness to meet applicable regulatory, quality and compliance standards.
  • Quality-focused, adept at developing good practices, open-minded to data-driven approaches and new digital solutions
  • International/ intercultural working skills


Preferred location is Cambridge, MA. Morristown, NJ and Vitry, France considered.

  • Bring the miracles of science to life alongside a supportive, future-focused team.
  • Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.
  • Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
  • Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks' gender-neutral parental leave.


The salary range for this position is:
$236,250.00 - $393,750.00

All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the LINK.

About Sanofi

Sanofi is a global pharmaceutical company that specializes in the research, development, and manufacturing of prescription drugs and vaccines. The company operates in over 170 countries and has a diverse portfolio of products that includes treatments for diabetes, cancer, cardiovascular disease, and rare diseases. Sanofi is committed to improving global health and has a strong focus on innovation and sustainability. The company has received numerous awards for its research and development efforts and is recognized as a leader in the pharmaceutical industry.
Learn more about Sanofi
Market Cap
$121.6 billion
Industry
Net Income
$12.3 billion
Founded
1990
5 Year Trend
+2.5%
Revenue
$37.3 billion
NASDAQ

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