Clinical Trials Lead Programmer
hace 1 mes
At Thermo Fisher Scientific, we are seeking a highly experienced and motivated Clinical Trials Lead Programmer to join our dynamic team. In this role, you will be responsible for overseeing the statistical and programming aspects of multiple projects, acting as the lead programmer, project lead, or project oversight lead for a client/asset. You will play a crucial role in the design, analysis, and reporting of clinical trials, ensuring adherence to regulatory requirements and industry standards.
Key Responsibilities
Serves as a lead programmer or project lead on selected studies or drug programs of all complexity and size scale.
Works directly with teams and clients to conduct team meetings, develop and maintain project timelines, assess and forecast resources needed, is accountable for study budgets and familiar with any relevant contractual obligations or limits with our clients.
May serve in a senior project oversight role on selected projects.
May serve in a contributor or reviewer role of key submission materials for regulatory authorities.
Provides general infrastructure support to the department.
Examples include representing the company at industry conferences, presenting/teaching at department meetings, establishing training materials for the department, contributing to documents or policies, and contributing to process improvement and department initiatives.
Increases knowledge base and professional skills for self and junior team members.
In areas including programming technology and techniques, clinical trials, and developments in the pharmaceutical industry.
Works to increase the visibility of the company.
Encouraging the publication of articles in industry journals and presentations at conferences.
May manage staff of small team.
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.
Requirements
Education:
MS/MA degree in computer science, statistics, biostatistics, mathematics or related field and at least 3 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 5 years of experience that provides the knowledge, skills, and abilities to perform the job requirements.
Experience:
Preferred is at least 6 years of clinical trial experience as a statistical programmer and at least 1 year of leadership experience.
Knowledge, Skills, Abilities:
Programming experiences for the studies in Clinical Pharmacology is strongly preferred. Good knowledge and background in statistics are preferred.
Additional Information
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation
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