Manager/Sr Manager Biostatistics & Programming

Thermo Fisher ScientificTaguig City, PhilippinesonsiteSalary not postedView the original posting at Thermo Fisher Scientific ↗

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Sr. Manager Programming – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. As part of our expert team, you’ll have the opportunity to ensure operational excellence that makes a real difference in clinical trials. As a Sr. Manager Programming, you will manage a team within the department who are responsible for the bioinformatics programming aspects of clinical trials from design through analysis and reporting. Provides project oversight of studies or sponsor programs and leadership for strategic client relationships and/or significant client portfolios. Acts as a key contact for client interactions and bid defenses, and ensures effective delivery across all project requirements including communicating priorities and work direction to complete assigned tasks on time and within budget. Able to act in the project oversight role on select projects. You will represent the department to clients on study matters, bid defenses, or submission of clinical data to regulatory authorities. You will directly contribute to proposals and bids, organize teams, and implement study strategies to ensure process and programming efficiencies. Additionally, you will be responsible for the creation and maintenance of programs for statistical report generation and program validation. What You’ll Do: • Manages staff, which may include interviewing and selection, job description preparation, professional development, goal setting, performance management, behavioral and technical coaching and mentoring, employee counseling, and separations. Approves courses of action on salary administration, hiring, corrective action, and terminations. Reviews and approves time records, expense reports, requests for leave, and overtime. Promotes all aspects of PPD Equal Employment Opportunity policy and Affirmative Action Plan. Assures department adherence to good scientific, ethical, and regulatory standards. • Reviews and ensures adherence to departmental working practice documents and SOPs, and contributes to their development. • Recommends strategies to senior management on ways to increase the knowledge base and professional skills of staff in areas including programming technology and techniques, clinical trials, and the pharmaceutical industry through on the job training, mentoring, and internal or external training courses. • Works to increase the visibility of the company by encouraging the publications of articles in industry journals and presentations and/or section chairing at conferences, and assists senior management in conducting reviews of publications to ensure they meet a high standard. • As needed, fulfills senior level project oversight roles for studies and/or works directly with project leads and client representatives to assess risks and issues related to project quality, timelines, and budget. • Provides general infrastructure support to the department. Examples include giving presentations at department meetings, contributing to documents or policies, contributing to and/or leading process improvement initiatives, and assisting with departmental web page development. Education and Experience Requirements: MS/MA degree in computer science, statistics, biostatistics, mathematics or related field and at least 7 years of experience that provides the knowledge, skills, and abilities to perform the job requirements, or Bachelor's degree in computer science, statistics, biostatistics, mathematics or related field or equivalent and relevant formal academic / vocational qualification, and at least 9 years of experience that provides the knowledge, skills, and abilities to perform the job requirements Preferred is at least 8 years of clinical trial experience as a statistical programmer and at least

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