Scientist II – Transporter Study Coordinator

PharmaronExton, PA
$65,000 - $75,000Onsite

About The Position

Pharmaron is seeking a highly motivated Scientist II – Transporter Study Coordinator to support regulatory In Vitro ADME studies and contribute to the continued growth of our DMPK capabilities. This role serves as a critical liaison across multidisciplinary teams to coordinate transporter studies supporting IND and NDA submissions while ensuring exceptional scientific quality, operational excellence, and client satisfaction. The successful candidate will operate independently outside of the laboratory while partnering closely with scientists and analysts to support study planning, execution, data interpretation, reporting, and client communications.

Requirements

  • Bachelor's or Master's degree in Biochemistry, Pharmacology, Microbiology, Molecular Biology, or related scientific discipline
  • Minimum 3 years of industry experience in molecular biology, pharmacology, biochemistry, DMPK, or related scientific fields
  • Experience supporting transporter studies, cell-based assays, or regulatory drug metabolism studies preferred
  • Previous project coordination or study management experience preferred
  • Working knowledge of: Cell biology and cell culture techniques, Drug metabolism and pharmacokinetics (DMPK), Transporter biology and drug-drug interaction studies, Regulatory expectations for ADME studies
  • Proficiency with: Microsoft Office Suite (Excel, Word, PowerPoint), GraphPad Prism, Scientific data analysis and reporting tools
  • Strong written communication skills with the ability to prepare high-quality scientific documentation
  • Strong organizational skills and exceptional attention to detail
  • Ability to thrive in a fast-paced, matrixed environment with multiple priorities
  • Self-motivated with strong problem-solving skills and scientific curiosity
  • Ability to manage multiple projects simultaneously while maintaining quality and timelines
  • Collaborative mindset with strong interpersonal and communication skills
  • Reliable attendance and commitment to supporting project deliverables and team objectives

Nice To Haves

  • Experience supporting transporter studies, cell-based assays, or regulatory drug metabolism studies
  • Previous project coordination or study management experience

Responsibilities

  • Coordinate and support regulatory In Vitro ADME studies, with a focus on transporter substrate and efflux studies supporting IND and NDA submissions
  • Collaborate cross-functionally with scientific teams to drive study execution and ensure timelines are met
  • Support studies conducted in accordance with ICH M12 guidance and sponsor-specific requirements
  • Plan study activities and proactively identify and resolve execution, scheduling, and operational challenges
  • Process, analyze, interpret, and communicate scientific data and study outcomes
  • Draft study protocols, reports, presentations, case studies, and client updates
  • Maintain accurate study records, documentation, and archive materials in accordance with regulatory requirements
  • Present findings and discuss scientific results with clients and sponsors
  • Ensure high-quality deliverables while maintaining strong attention to detail and customer focus
  • Stay current with evolving global regulatory expectations and industry trends related to drug discovery and development
  • Participate in internal research initiatives and continuous improvement projects
  • Attend project meetings, progress reviews, and departmental activities
  • Support additional scientific or operational activities as assigned

Benefits

  • Medical, Dental & Vision insurance with significant employer contributions
  • Employer-funded Health Reimbursement Account
  • Healthcare & Dependent Care Flexible Spending Accounts
  • 100% Employer-paid Employee Life and AD&D Insurance, Short and Long Term Disability Insurance
  • 401k plan with generous employer match
  • Access to an Employee Assistance Program
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