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Senior Statistician – Real World Data Analytics Consultant

United States

 

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds….

ClinChoice is searching for a Real World Statistics Contractor to join one of our clients. 

ClinChoice is a leading global CRO, dedicated to supporting clinical trials and real-world evidence research with a focus on exceptional quality, career development, and a supportive culture. As we expand our presence and offerings, we’re looking for an experienced Real World Statistics Contractor to join our dynamic team and lead analytical efforts across diverse therapeutic areas for a high-profile sponsor.

General Summary:

The Real World Statistics Contractor will serve a Statistics role on assigned projects including real world observational studies, market access and reimbursement activities, clinical trials, and other ad hoc analyses conducted by Global Medicines Development and Affairs, and Commercial and Strategic Management. The individual will complete assigned work in a resourceful, self-sufficient manner, and should possess a good knowledge of related disciplines while performing statistics activities with a drug developer mindset.

Key Duties and Responsibilities:

The Real World Statistics Contractor:

  • Is responsible for all scientific and operational statistical work for assigned observational studies, real world data investigations, or clinical trials. Performs critical review of study protocols including study design and analysis methods, performs critical review of data and analysis results, conduct statistical analysis, and undertakes new and complex issues with some mentoring and guidance.
  • Participates in regular Study Execution Team meetings, representing Real World Statistics as a member of cross functional teams, providing strategic input and expert technical guidance to team members.
  • Effectively collaborates with multiple stakeholders from Health Economics and Outcome Research, Medical Affairs, Clinical Development and Real World Evidence teams.
  • When needed, supports development of study documents owned by Statistics such as Cross-functional Data Review plan, Key Results Memo, and Data Dissemination Plan in order to facilitate the review, summary, and dissemination of key study data/results.
  • When collaborating with statistical programming for deliverables, provides input into the programming specifications and perform critical review. Collaborates with statistical programming and other functions to ensure timely delivery of TFLs with high quality.
  • Contributes to study reports, publications, and related processes.

Knowledge and Skills:

  • Demonstrated ability to design and analyze observational studies with knowledge of US healthcare system, health insurance billing data, and electronic medical record data.
  • Strong programming skills; familiarity with data analysis methods.
  • Ability to work effectively in a constantly changing, fast-paced, diverse, and matrix environment.
  • Ability to multitask; strong work ethic and a "can-do" mentality.
  • Ability to show critical thinking with logical problem-solving.
  • Excellent written and verbal communication skills.
  • Excels in a team environment.
  • Collaborates well with non-statisticians.

Education and Experience:

  • Master or PhD degree in Biostatistics or related fields with 3 to 7 years of relevant work experience.
  • Minimum 2 years of experience working on observational studies within the life sciences industry or relevant academic, government, or consulting environment.
  • 3 years SAS and R programming experience is required.

The Application Process

Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step.  Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.

Who will you be working for?

About ClinChoice

ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.           

Our Company Ethos

Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology.   The success of these core values is evidenced by our below industry average turnover rates.

ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.


#LI-TT1 #LI-Remote #Senior #Contract

 

 

 

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