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ThermoFisher Scientific Senior Biostatistician in Cambridge, Massachusetts

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life – To enable our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. As part of our clinical research portfolio, our CorEvitas evidence-based solutions specialize in generating data intelligence and clinical insights needed to bring safe and effective treatments to market. Your objectivity and dedication to patient safety will improve health outcomes that people and communities depend on – now and in the future.

Location/Division Specific Information

Remote, USA

A key member of the CorEvitas Biostatistical Team, the Senior Biostatistician is the statistical team lead on many company projects. This role is directly responsible for the success of specific statistical deliverables. The multifaceted role requires interaction with academic affiliates, clients, various scientific resources, clinical principal investigators and project staff.

#CorEvitas

Discover Impactful Work:

Senior Biostatistician brings statistical expertise for performing analyses such as investigating prescribing patterns, comparing effectiveness between treatments and investigating differences in safety outcomes.

The CorEvitas Biostatistics team at CorEvitas has three major focuses of query work, pharmacovigilance (PV) work and registry coordination.

With query work, we design, analyze and report on research projects, aka queries, with our clients to produce publications for the public domain (e.g. abstracts, posters, podium presentations, manuscripts, etc.) Each query is a team effort that consists of this individual (biostatistician lead) who designs and leads analysis, biostatistician who performs the analysis, clinical epidemiologist who helps with design and frames the overall message and clinical research manager that coordinates the project.

Our pharmacovigilance (PV) work consists of close collaboration with the PV team in which we design, analyze and report on long-term post approval safety studies with our pharma clients to provide real-world evidence regarding safety.

With our registry coordination, we work cross-functionally with the Engineering, Clinical Data Management and Project Management teams on all the registry data taking into account client requests from our query and PV work.

A day in the Life:

Responsible for collaborating with investigators with diverse backgrounds to develop Statistical Analysis Plans (SAPs) that meet the requirements of the client research aims

Responsible for development and dissemination of final analytic reports to clients

Leads client-facing conversations regarding statistical aspects of client research projects

Makes original contributions to research projects, takes initiative in professional activities and makes sound statistical decisions on an independent basis

May oversee one or two members of the Biostatistical team (typically comprised of Biostatistician I/II/III) to complete the analyses detailed in the SAP, provide direction based on project requirements and ensure accuracy in maintaining data and program documentation

Provide guidance and procedures to biostatistical group for data management and data integration

Develop standardized algorithms and templates to create efficient and consistent statistical analyses

Participation in a variety of weekly conference calls with clients, internal teams and senior Biostatistical staff

Contribute and present published abstracts at research conferences and play a key role in published peer-reviewed manuscripts

Performs sample size and power calculations for use in protocol development

May train individuals within the department

Keys to Success:

Education

Doctorate or Masters’ with appropriate experience level education in Biostatistics, Statistics or Mathematics (or equivalent) is required

Experience

Minimum 3-5 years of post-doctorate experience (for PhD) or comparable experience for Masters-level candidate in a research or medical setting

Documented collaborative research experience with publications in peer-reviewed journals

Demonstrated knowledge of retrospective and prospective observational study designs and related methodology

Knowledge, Skills, Abilities

Knowledge of medical terminology and clinical epidemiology preferred

Must be highly proficient in at least one of the following statistical packages: R (preferred), SAS and/or Stata

Must be very familiar with complex, longitudinal data

Strong interpersonal skills are required

Demonstrated analytic skills to problem solve effectively

Strong scientific, leadership and communications skills as well as a strict adherence to ethical business and research practices

Must be able to make independent judgments under general supervision

Must be highly organized and detail-oriented, with excellent time management skills and the ability to multi-task

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

Apply today! http://jobs.thermofisher.com

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Accessibility/Disability Access

Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1-855-471-2255*. Please include your contact information and specific details about your required accommodation to support you during the job application process.

*This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

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