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Pharma R Jobs in Boston, MA (NOW HIRING)

Cytel

Senior Programmer FSP - RWD/EPI

Cambridge, MA · On-site +1

... for pharma industry, CRO, or academic institution * Intermediate to expert level proficiency in SQL is a must. In addition, SAS or R proficiency is required * Deep expertise analyzing RWE data ...

Instylla

Manufacturing Engineer II

Bedford, MA · On-site

$76K - $98K/yr

... Gage R&R). Preferred Skills: * Excellent hand/eye coordination and specific vision abilities ... Experience with chemical processing, such as pharma manufacturing or similar. * Inspection ...

Instylla

Manufacturing Engineer II

Bedford, MA · On-site

$77K - $110K/yr

... Gage R&R). Preferred Skills: * Excellent hand/eye coordination and specific vision abilities ... Experience with chemical processing, such as pharma manufacturing or similar. * Inspection ...

Instylla

Manufacturing Engineer II

Bedford, MA · On-site

$76K - $98K/yr

... Gage R&R). Preferred Skills: * Excellent hand/eye coordination and specific vision abilities ... Experience with chemical processing, such as pharma manufacturing or similar. * Inspection ...

Verastem

Medical Director, Clinical Development

Boston, MA · On-site

$250K - $310K/yr

... team and R&D. Lead and present at investigator meetings and advisory committees. * Maintains ... D. or equivalent) required. * 3+ years of experience in biotech / pharma industry oncology drug ...

BICO

Field Service Engineer - (Woburn, MA region)

Woburn, MA · On-site +1

$86K - $108K/yr

... R&D. - Travel up to 80% overnight as required. - Other duties as assigned. What We Are Looking For ... in pharma and biotech.With 53,600+ instruments installed in over 65 countries, BICO products ...

Actithera

Head of Clinical Affairs

Cambridge, MA · Remote

$150K - $275K/yr

... pharma, with experience in oncology or radiopharmaceuticals. Expertise in authoring ICH-compliant documents (IB, SAP, CSR) and proficiency in data visualization tools (e.g., GraphPad, R). Strong ...

MMS

Study Design Statistician (US)

Boston, MA · On-site

... pharma, CRO, academic). * Willingness to engage with clients to understand and research problems ... Experience in SAS and/ or R statistical software packages. * Experience in study design and ...

Genentech

Head of Product Biometrics

Boston, MA

$182K - $339K/yr

Act as a strategic liaison between business functions and R&D. * Manage a complex ecosystem of ... years in Pharma/Biotech Biometrics domain and 4+ years in a leadership role managing ...

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All JobsPharma R JobsPharma R Jobs in Boston, MA

Pharma R information

What is a Pharma R?

Pharma R professionals are individuals who work in pharmaceutical research and development (R&D). They are responsible for discovering, developing, and testing new drugs and therapies to ensure they are safe and effective for patients. Their roles may include designing experiments, conducting clinical trials, analyzing data, and complying with regulatory standards. Pharma R professionals often work with interdisciplinary teams, including scientists, clinicians, and regulatory experts. Their work is crucial in bringing new medicines to market and advancing medical science.

What are the key skills and qualifications needed to thrive as a Pharma R?

To thrive as a Pharma R (Pharmaceutical Representative), you need a solid understanding of pharmaceutical products, medical terminology, and sales principles, often supported by a bachelor's degree in life sciences or a related field. Familiarity with CRM software, data analysis tools, and regulatory compliance systems is typically required. Strong interpersonal, negotiation, and presentation skills help build relationships with healthcare professionals and stand out in the role. These capabilities are vital for effectively promoting pharmaceutical products, ensuring regulatory adherence, and achieving sales targets in a competitive industry.

What are some common challenges faced by Pharma R professionals when working cross-functionally with other departments?

Pharma R professionals often collaborate closely with teams such as clinical research, regulatory affairs, and marketing. A common challenge is aligning priorities and timelines across departments with different objectives and regulatory requirements. Effective communication and proactive planning are essential to ensure that scientific data, compliance standards, and commercial strategies are integrated smoothly. Building strong relationships and understanding each team's unique constraints can help navigate these complexities and lead to more successful project outcomes.

What is the difference between Pharma R vs Pharma Associate?

AspectPharma RPharma Associate
Required CredentialsBachelor's degree in pharmacy, chemistry, or related field; licensing may be requiredAssociate degree or diploma in pharmacy technology or related field
Work EnvironmentResearch labs, pharmaceutical companies, clinical trial sitesRetail pharmacies, hospital pharmacies, pharmaceutical manufacturing facilities
Employer & Industry UsagePrimarily in research and development within pharma companiesInvolved in dispensing, patient interaction, and pharmacy operations

Pharma R roles focus on research, development, and clinical trials, requiring specialized scientific credentials. Pharma Associates typically work in pharmacy settings, handling medication dispensing and patient care. While both roles are essential in the pharmaceutical industry, Pharma R is research-oriented, whereas Pharma Associate is more operational and patient-facing.

What are popular job titles related to Pharma R jobs in Boston, MA?

For Pharma R jobs in Boston, MA, the most frequently searched job titles are:

What job categories do people searching Pharma R jobs in Boston, MA look for?

The top searched job categories for Pharma R jobs in Boston, MA are:

Pharma R jobs near you

Senior Statistical Programmer FSP - RWD/EPI

Cytel

Cambridge, MA • On-site, Remote

Full-time

Posted 15 days ago

Job description


You will contribute by:
  • Providing support to the Epidemiology team by preparing Real World data, advising on data analytic strategies, and supporting stakeholders in various epidemiology analytic activities
  • Programming and conducting statistical analysis under the direction and supervision of epidemiologists/statisticians including data coding, creation of algorithms, linkage of datasets, and use of statistical packages or platforms
  • Supporting statistical programming to generate innovative means of data standardization, visualization, and reporting of observational data
  • Supporting Medical Affairs (e.g. observational studies leveraging RWD); Global Patient Safety and Risk Management (e.g., analysis to obtain background rates) for the development of regulatory/safety documents, and Clinical Development (e.g.; assessment of patient populations/ protocol feasibility)
    • The position will partner with Epidemiologists to manage relationships with internal and external stakeholders
  • Being able to prioritize and manage work across multiple projects and stakeholders
  • Providing strong communication to ensure successful and timely project delivery
  • Solving technical problems with experience and expertise

Responsibilities
Summary of Key Responsibilities:
  • Assist in development of study protocols and analysis plans leveraging large RWD sources (Claims and/or EHR)
  • Liaise with data vendors to obtain relevant data extracts for research studies consistent with study protocols
  • Create analytical databases from data extracts to facilitate conduct of data analyses
  • Conduct analyses consistent with methods set forth in study protocols and analysis plans
  • Produce tables and figures for discussions with other investigators, clients, and for study reports
  • Present results internally and to clients
  • Assist in the preparation of study reports and other deliverables
  • May have supervisory responsibilities in the future

Qualifications
What we're looking for:
  • Master's degree or PhD in related field (epidemiology, biostatistics, statistics, bioinformatics, economics) and 5+ years of experience conducting RWE analytics for pharma industry, CRO, or academic institution
  • Intermediate to expert level proficiency in SQL is a must. In addition, SAS or R proficiency is required
  • Deep expertise analyzing RWE data sources such as Optum (Clinformatics Datamart® and Market Clarity), Truveta and UK Biobank. Experience analyzing clinical trial and/or registry data is desirable
  • Familiarity with relational databases and proficient understanding of claims and ancillary file layouts
  • Experience with applied statistics including regression analysis (OLS, longitudinal, logistic, Cox, GLM/GEE), survival analyses (Kaplan-Meier, cumulative incidence, accelerated failure time models), and propensity weighting
  • Excellent project management skills; can prioritize multiple tasks and goals to ensure timely completion
  • Confident and competent when interacting with internal and external stakeholders
  • Strong written/verbal communication skills. Highly effective at summarizing and presenting key considerations and evidence

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