Position: Pharmacologist ADME / DMPK specialist/toxicology specialist Experience Level: Ph.D. in Biochemistry/Biology/Cell Biology/Pharmacokinetics/Pharmacology or a related scientific field. Entry level to 5 years relevant industrial R&D experience. Location: Remote (India, Philippines, Spain, Vietnam) Company Description: LegalForce RAPC Worldwide P.C. (parent law firm of Trademarkia) is expanding its Life Sciences practice to support clients developing cutting edge pharmaceutical and AI driven drug discovery innovations. We are building a specialized Pharmacology & AI Driven Drug Development team. With AI transforming pharmacokinetics (PK), pharmacodynamics (PD), and drug efficacy modeling, our clients need expert scientific support to secure strong patent protection, navigate regulatory pathways, and accelerate drug development. Role Descriptions (2): (1) ADME / DMPK specialist: Seeking a scientist interested in the discovery and clinical development of medicines including small molecules, biologics/antibodies, peptides, ADCs, siRNAs, gene therapies, and other complex modalities. You will serve as a technical innovator in cross functional teams to deliver novel therapies to patients. This role requires engaging in experimental design and data interpretation to deliver the discovery and development portfolio of investigational targets and novel therapeutics. We support one another through shared learning and mutual responsibility for the enterprise of making medicines. You will: Innovate in a multidisciplinary collaborative environment with primary responsibility for ADME studies to support preclinical and clinical development of the clients portfolio across modalities including small molecules, biologics/antibodies, peptides, ADCs, siRNAs, gene therapies and other complex modalities Design and implement hypothesis driven studies to answer ADME, PK/PD and clinical pharmacology questions Be accountable for the delivery of scientifically integrated data packages to guide compound selection, study design, portfolio decisions, and regulatory submissions Partner with cross functional colleagues in both Discovery and Development (eg. Toxicology, Pharmacology, Chemistry, Clinical PK/PD, Clinical Pharmacology, Regulatory, and Medical) to assess drugability and optimize ADME properties to deliver drug candidates to the clinic, as well as to design and support nonclinical and clinical studies supporting global registration packages Integrate in vitro, in vivo, and in silico ADME data to define structure activity and structure property relationships and deliver favorable molecular and experimental design strategies to guide drug delivery and optimization Engage, innovate, and collaborate with colleagues and interdisciplinary teams Lead the preparation of regulatory communication, patent applications, and documents to support clinical development, new drug applications (NDA and BLA) and line extensions and interact with regulatory agencies