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Health Care 🏢 Full Time ⭐️ Verified

Senior Pharmaceutical Scientist

BioInnovate Therapeutics
Cambridge
Salary Estimate
USD 135.000 – USD 165.000
Live Update
25 Mei 2026
Deadline
25 Mei 2027

Job Description

Join BioInnovate Therapeutics, a leader in biopharmaceutical innovation, as we pioneer next-generation therapies for rare diseases. We're seeking a passionate Senior Pharmaceutical Scientist to drive our drug discovery pipeline from concept to clinical trials. Our state-of-the-art Cambridge facility offers unparalleled resources and collaborative opportunities to transform healthcare.

At BioInnovate, you'll work alongside Nobel laureates and industry veterans in a culture that values scientific rigor and creative problem-solving. We offer competitive compensation, comprehensive benefits, and flexible work arrangements to support your professional growth and personal well-being.

Responsibilities

  • Lead cross-functional teams in designing and executing preclinical drug development studies
  • Develop and optimize analytical methods for compound characterization and stability testing
  • Prepare regulatory documentation (IND/CTD) ensuring compliance with FDA/EMA guidelines
  • Conduct thorough literature reviews and patent landscape analysis for novel therapeutic targets
  • Mentor junior scientists and supervise lab operations including GLP compliance
  • Collaborate with CROs to manage outsourced preclinical and clinical trial activities
  • Present research findings at international conferences and peer-reviewed publications

Qualifications

  • PhD in Pharmaceutical Sciences, Chemistry, or related field with 5+ years industry experience
  • Expertise in small molecule drug development and formulation strategies
  • Proven track record in regulatory affairs and compliance documentation
  • Strong proficiency in HPLC, LC-MS, and spectroscopic analytical techniques
  • Demonstrated experience with preclinical study design and data interpretation
  • Excellent project management skills with ability to handle multiple timelines
  • Validated knowledge of GMP/GLP principles and ICH guidelines
  • Exceptional communication and leadership abilities

Required Skills

Drug Development Regulatory Affairs Analytical Chemistry GMP Preclinical Studies HPLC LC-MS Formulation CRO Management

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