Scientist II - Regulatory In Vitro ADME (Transporter Studies)

Position:

Scientist II - Regulatory In Vitro ADME (Transporter Studies)

Location:

Exton, PA Salary Range :

$65,000 - $75,000 About Pharmaron Pharmaron is a global CRO (Contract Research Organization) helping pharma and biotech companies bring new therapies to life. With over 21,000 employees worldwide across 23 locations in the US, UK and China, we support drug discovery through to manufacturing with fully integrated, high-quality services. We're proud of the impact we make and just last year, we supported over 780 discovery projects , 1,000+ CMC programs , and 1,000+ clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,000 global customers . To learn more, visit . Job Overview Pharmaron is seeking a highly motivated Scientist II - Regulatory In Vitro ADME (Transporter Studies) 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. Key Responsibilities Study Coordination & Scientific Support 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 Documentation & Client Support 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 Additional Responsibilities 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 What We're Looking For 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 What Makes You Successful 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 Physical & Work Environment Requirements On-site position located in Exton, PA Ability to sit or stand for extended periods in office and laboratory environments Ability to work in varying laboratory and office conditions, including changing temperatures, lighting, and noise levels Visual acuity required for reviewing protocols, interpreting data, and analyzing graphs and reports Why Pharmaron? Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R D solutions to its partners in North America, Europe, Japan, and China.

Collaborative Culture:

You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.

Benefits:

As part of our commitment to your well-being, we offer a comprehensive benefits package: Insurance including Medical, Dental & Vision 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 How to

Apply:

Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today! As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.