Job Directory Senior Modeling and Simulation Analyst / Senior Modeling and Simulation Analyst Project Lead

Senior Modeling and Simulation Analyst / Senior Modeling and Simulation Analyst Project Lead
South San Francisco, CA

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Job Description

RESPONSIBILITIES

The Clinical Pharmacology Department within Development Sciences at Genentech, Inc. is seeking an experienced Statistical Programmer to join the Modeling and Simulation Analyst (MSA) group at the South San Francisco site. This individual will utilize a variety of analytic software such as SAS, R, or S-Plus to integrate PK drug concentration-time measures, pharmacodynamic responses, and clinical safety and efficacy information for pharmacometric Modeling and Simulation (M&S) analyses. This role will work with and potentially manage other colleagues within a high-performing team environment. This individual will be accountable for activities including data programming, effective resourcing, efficient operations, timely delivery, quality assurance, and regulatory compliance. He/she must be an effective communicator and efficient at working within a distributed team environment. Additional responsibilities will include set-up and maintenance of systems for programming, data access, sharing, and storage. He/she will also take the initiative to identify gaps and lead the development of standardization, process optimization, and workflow automation. This will be accomplished by working in close partnership with both internal and external teams. This role requires strong leadership skills and the ability to influence. Candidate may be responsible to manage employees via direct and/or matrix management, providing oversight of project deliverables as well as team and department initiatives.

EXPERIENCE

We are looking for a candidate with 9+ years of experience in a clinical programming environment with an extensive record of on-the-job success. Preference will be given for candidates with pharmacokinetic/pharmacodynamic data experience. Qualified candidates will have solid hands-on expertise in SAS and R programming for various types of clinical trial data. Rich knowledge of the drug development process, clinical data systems, and CDISC data standards is required. Experience in generating analysis datasets, data pooling and graphical representation of data as well as working experience with M&S datasets, methodologies, and software (such as NONMEM) is highly desired. The candidate must have strong communication skills, interpersonal skills, people management skills, and leadership skills including motivation, delegation, and conflict management in a fast-paced multi-tasked matrix environment. The candidate should demonstrate a history of process optimization within the context of an efficient team environment. The candidate should have the ability to establish and maintain effective working relationships with cross-functional team members. Good project planning and organizational skills are essential. People management experience is highly desired.

EDUCATION

B.S., M.S., or equivalent in Statistics, Mathematics, Pharmacometrics, Engineering, Data Science, or related discipline.

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