Job Description
Let’s talk about some of the key responsibilities of the role:
- The Associate Director, Biostatistics possesses a unique combination of expert statistics support and systems and compliance.
- Ownership of all scientific and operational statistical work for assigned clinical trials. Implements design and analysis methods.
- Responsible for presenting data reviews as needed in ET and upper management circles.
- Oversee programming and track the status with respect to performance metrics, deliverables, and timelines.
- Develops study Statistical Analysis Plans, including table, figure, and listing (TFL) shells.
- Develops study documents such as data review plan, Topline Results plan, and Data Dissemination Plan to facilitate the review, summary, and dissemination of key study data/results.
- Provide statistical expertise in support of interactions with regulatory agencies such as the FDA to include pre-submission meetings/questions, responses to regulatory agency questions, face-to-face meetings with regulators, etc.
- Accountable for overseeing performance of external vendors responsible for statistical work and deliverables to ensure quality completion of clinical data related deliverables.
- Participate in the development of policies, SOPs, work instructions, and clinical development process improvements relating to statistics.
- Validate software, in the role of system owner or tester, and test SAS Macros and other programs, maintaining the required validation and testing documentation.
- Provide support to implementation and maintenance of clinical data visualization tools, such as JReview.
- Manage multiple and varied tasks, prioritize workload with attention to detail.
- In addition to the above employees are required to carry out any reasonable request to perform other duties as may be required within the scope of the job title.
Factors for Success:
- A professional statistician (including a Statistics MS / PhD), with design and analysis consultancy skills and knowledge across a broad range of applications.
- Minimum of Master’s Degree +10 years of experience, Or PhD +8 in the medical device, pharmaceutical, biotech or CRO industry is required.
- Experience with ophthalmology therapeutics and interface with FDA/regulatory agencies is highly desirable.
- Ability to work cross-therapeutic areas preferred.
- Proficiency in statistical programming including but not limited to SAS.
- Knowledge of FDA Regulations and ICH/GCP Guidelines.
- Proven experience handling confidential and sensitive information with the ability to exercise discretion and show good judgment, honesty, integrity, and trust building behaviors in all dealings is essential and required.
- Ability to work collaboratively to project plan, problem-solve and deliver results.
- Must have excellent customer-service orientation, high degree of professionalism and ability to work with limited direction.
- Self-motivated, with initiative and the ability to take ownership of and follow through with assigned tasks.
- Ability to multi-task and shift priorities quickly while working under tight deadlines.
A Few Other Details Worth Mentioning:
- The position will be based in our beautiful Irvine office, complete with a courtyard, snacks, drinks, and occasional catered meals. We provide a hybrid work environment. Remote work is an option.
- This position reports directly to our Director, Biostatistics
- Some travel may be required – up to 20%
At Tarsus, we understand the importance of attracting and retaining top talent. The expected base pay range for this position is $165,000 - $231,000 plus bonus, stock equity, and comprehensive benefits. The base pay range reflects the target range for this position, but individual pay will be determined by additional factors such as job-related skills, experience and relevant education or training. Our benefits include health, dental and vision insurance benefits to ensure your well-being. We believe in work-life balance and offer generous paid time off, including vacation, holidays, and personal days. For more details regarding Tarsus benefits, please visit: https://eb.alliant.com/26tarsusbenefitssnapshot.
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Tarsus Pharmaceuticals, Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.
