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Director/Sr. Director, Clinical Pharmacology

$225k - $315k

Scholar Rock

Cambridge, MADevelopment – Clinical Pharmacology /Full-Time /On-siteScholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.Summary of Position:Scholar Rock is seeking a motivated, energetic, and outstanding individual with experience in clinical pharmacology and pharmacometrics to join our team in developing novel biologic therapies that target protein growth factors in the disease microenvironment. The Director/Senior Director of Clinical Pharmacology, reporting to the Head of Clinical Pharmacology, will have strong quantitative clinical pharmacology skills and hands-on modeling and simulation experience. This individual will be responsible for the analysis and interpretation of PK, PD, and efficacy data to guide the development of biologics including monoclonal antibodies. Position ResponsibilitiesLead clinical pharmacology strategies across multiple programs at various stages of clinical developmentExecute modeling and simulation plans including PK/PD, population PK, and exposure-response analyses to guide clinical trial design, dose selection and optimizationDevelop IV to SC transition dosing plansProvide pediatric clinical pharmacology expertise and co-lead workstreams related to formulation development and sub-cutaneous route of administration Apply model-based drug development principles to answer key development questions enabling efficient drug developmentContribute to preparation of regulatory documents and participate in discussions with Regulatory Agencies, with a focus on Model-informed Drug Development (MIDD).Contribute to clinical protocol design, study execution, data analysis, and writing clinical study reportsCollaborate and mentor bioanalytical and translational team to develop comprehensive preclinical and clinical PK/PD strategyCandidate RequirementsPhD in pharmacokinetics or pharmacology7-10 years of experience in pharma/biotech industry, with proven track record of using clinical pharmacology to guide clinical trial/dosing decisionStrong background in quantitative drug development and a desire to work collaboratively across different functional areas, as well as with external vendors and partnersExperience in modeling and simulation of pharmacokinetic, pharmacodynamic, and exposure-response analyses, including expertise with population modelingAbility to interpret and integrate complex data sets across multiple disciplines including pharmacology, DMPK, toxicology assessing the clinical relevanceStrong interpersonal writing and presentation skills, as well as the ability to function in a team environment are essentialUnderstands the drug development process from pre-IND through BLAHighly organized, outcome-oriented, self-motivated performer$225,000 - $315,000 a yearScholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Vacancy posted 1 day ago
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