Senior Research Associate & Group Leader - DMPK

Perform routine in vitro ADME assays such as microsomal stability, plasma stability, solubility, permeability, CYP inhibition, and plasma protein binding assays

Develop, optimise, and execute analytical methods using LC-MS/MS and complementary detection modalities (absorbance/fluorescence-based assays)

Support development and validation of new ADME assays to expand the group’s scientific capabilities

Process and analyse experimental data using GraphPad Prism, MS Excel, and mass spectrometry software platforms (e.g., Sciex)

Prepare clear experimental documentation, study summaries, and reports for internal teams and external collaborators

Coordinate with third-party collaborators for pharmacokinetic (PK) studies, including in vivo animal studies where applicable

Present experimental results and scientific observations in internal meetings, project reviews, and cross-functional discussions

Work closely with colleagues across biology, and ADME groups to provide integrated drug discovery support alongside chemistry teams

Support laboratory operations including reagent ordering, inventory management, assay consumables tracking, and coordination of laboratory logistics

Master's in Lifescience with 4-5 years of working experience with LC-MS/MS, HPLC, bio-analytical studies etc.

Strong understanding of laboratory techniques, analytical instrumentation, and underlying scientific principles

Practical experience working in biotechnology laboratories including cell culture facilities and in vitro ADME assay environments

Good theoretical and practical knowledge of cell culture systems (established cell lines) and ADME assays such as microsomal stability, permeability, CYP inhibition, plasma stability, and plasma protein binding

Ability to troubleshoot experimental challenges and apply sound scientific judgment

Self-driven and capable of managing multiple tasks while working within demanding project timelines

Strong attention to detail and commitment to maintaining high scientific and data quality standards

Excellent interpersonal skills with the ability to collaborate effectively across multidisciplinary teams

Strong communication skills for interacting with internal teams, collaborators, and stakeholders

Highly organised with the ability to function effectively in a fast-paced research environment

Curiosity, enthusiasm for science, and a desire to contribute to innovative drug discovery programs

A positive and collaborative mindset with the ability to contribute to a supportive and high-performance team culture at o2h

Lead, mentor, and develop a team of scientists engaged in In-Vitro ADME/DMPK studies.

Oversee the design, execution, analysis, and interpretation of In-Vitro ADME studies, including metabolism, transporter, and drug-drug interaction assessments.

Manage external CRO partnerships for In-Vivo PK studies, ensuring timely execution, data quality, and delivery.

Provide scientific guidance and DMPK strategies to support drug discovery and development projects.

Analyze and interpret study data, prepare technical reports, and present findings to internal and external stakeholders.

Serve as the primary scientific point of contact for clients, ensuring effective communication and project delivery.

Support proposal preparation, project scoping, contract review, and project onboarding activities.

Manage study budgets, resource allocation, and operational efficiency.

Drive continuous improvement initiatives and implement best practices across DMPK operations.

Collaborate closely with cross-functional teams to integrate ADME/DMPK data into project decisions.

Prepare and present monthly MIS reports, including project status, resource utilization, risks, and key performance metrics.

Ph.D. in Pharmaceutical Sciences, Pharmacology, or a related Life Sciences discipline.

10–15 years of relevant experience in DMPK, In-Vitro ADME, and Pharmacokinetic sciences within pharmaceutical, biotechnology, or CRO organizations.

Proven experience in leading scientific teams and managing complex research projects.

Strong expertise in In-Vitro ADME studies and interpretation of DMPK data.

Experience managing CRO collaborations and outsourced In-Vivo PK studies.

Excellent leadership, project management, communication, and stakeholder management skills.

Strong analytical and problem-solving capabilities with a client-focused approach.

Ability to communicate complex scientific concepts effectively to diverse audiences.