Discover Exciting Career Opportunities in Clinical Statistics and Programming

What do clinical statisticians and programmers do?

Clinical statisticians and programmers play a critical role in healthcare and pharmaceutical research. They analyze clinical trial data, ensure data integrity, and develop statistical models to support evidence-based medical decisions, drug development, and regulatory compliance.

What are the duties associated with the role of clinical statistics and programmer?

Duties associated with the role of clinical statisticians and programmers include:

Data Analysis: Analyzing and interpreting clinical trial data to draw meaningful conclusions and insights
Statistical Modeling: Developing and applying statistical models to assess the effectiveness and safety of medical treatments
Data Management: Ensuring the quality and integrity of clinical trial data through data cleaning and validation
Protocol Development: Collaborating with researchers to design statistically sound clinical trial protocols
Regulatory Compliance: Ensuring adherence to regulatory requirements and standards, such as FDA guidelines
Statistical Programming: Writing and implementing code for data analysis and reporting
Safety Monitoring: Monitoring and analyzing adverse events and safety data during clinical trials
Statistical Reporting: Preparing reports, summaries, and documentation for regulatory submissions
Data Visualization: Creating visual representations of data to aid in decision-making and communication
Quality Control: Conducting quality control checks to ensure accuracy and consistency in analysis
Cross-functional collaboration: Collaborating with cross-functional teams, including clinical researchers and data managers
Statistical Consultation: Providing statistical expertise and guidance to support clinical trial design and analysis
Validation and Testing: Validating statistical programs and conducting testing to ensure accuracy
Continuous Learning: Staying updated with industry trends, methodologies, and regulatory changes
Ethical Conduct: Adhering to ethical and confidentiality standards in handling sensitive clinical trial data

These responsibilities are vital for generating reliable and scientifically rigorous outcomes in clinical research and pharmaceutical development.

Get career advice for clinical statisticians & programmers

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What are the average salaries for clinical statisticians and programmers in US?

Average Base Salary

$84,241

Per Year

$57K$116k

The average salary for Clinical Statistics and programmers is $84,241 per year in the United States.

How much do similar professions get paid in the United States?

Epidemiology Manager

Job openings

Average $45 per hour

Frequently Asked Questions about Clinical Statistics & Programmers

Clinical statisticians and programmers typically work in office settings, often within pharmaceutical companies, research institutions, or healthcare organizations. They collaborate with multidisciplinary teams, including researchers, data managers, and regulatory experts, in a fast-paced and detail-oriented environment. Remote work options are also common, providing flexibility in the work setting.

Clinical Statisticians and programmers can advance their careers by pursuing advanced degrees (Ph.D.), gaining diverse clinical trial experience, seeking certifications (e.g., SAS Certified Clinical Trials Programmer), and staying updated with industry trends and regulatory changes. Networking, mentorship, and pursuing leadership roles also enhance career growth.

Skills essential for clinical statisticians and programmers include proficiency in statistical analysis, expertise in statistical software (e.g., SAS, R), knowledge of clinical trial methodologies, data management, regulatory compliance, and effective communication to collaborate with cross-functional teams. Adaptability and continuous learning are crucial in this dynamic field.

Yes, there are certifications available for clinical statisticians and programmers, such as the SAS Certified Clinical Trials Programmer and the Certified Clinical Data Manager (CCDM) certification. These certifications validate expertise in data management and analysis within the clinical research domain.

The career outlook for clinical statisticians and programmers is promising. With the growing emphasis on evidence-based healthcare and pharmaceutical research, demand for their expertise in clinical data analysis and regulatory compliance is expected to remain strong. Opportunities exist in pharmaceutical companies, healthcare institutions, research organizations, and regulatory agencies. Continuous learning and staying updated with industry trends will be key to long-term success in this field.

Clinical Statistics & Programmer Salary in the United States

Average Base Salary

$84,241

Per Year

$57k$116k

The average salary for Clinical Statistics and programmers is $84,241 per year in the United States.

100%

Salary satisfaction

Based on 6,077 ratings

The job of project manager (unspecified type / general) has received job satisfaction.

How much do similar professions get paid in the United States?

Epidemiology Manager

Job openings

Average $45 per hour

How to Become a Clinical Statistician and Programmer

To become a clinical statistician and programmer, follow these steps:

Educational Foundation:
- Obtain a bachelor's degree in statistics, mathematics, computer science, or a related field.
- Consider pursuing an advanced degree (master's or Ph.D.) in biostatistics, statistics, or a closely related discipline for more specialized roles.
Statistical Skills:
- Develop a strong foundation in statistical concepts, including hypothesis testing, regression analysis, and experimental design.
Programming Proficiency:
- Learn statistical programming languages such as SAS, R, or Python.
- Gain expertise in data manipulation and analysis using these languages.
Clinical Knowledge:
- Familiarize yourself with clinical trial methodologies, terminologies, and regulatory requirements.
- Understand the drug development process and the role of statistics in clinical research.
Data Management:
- Acquire data management skills to handle and clean clinical trial data effectively.
Statistical Software:
- Become proficient in using statistical software packages and tools commonly used in clinical research.
Regulatory Compliance:
- Learn about regulatory guidelines and compliance requirements relevant to clinical trials (e.g., FDA, ICH GCP).
Clinical Data Analysis:
- Gain experience in analyzing clinical trial data, including safety and efficacy assessments.
Communication Skills:
- Develop effective communication skills to convey complex statistical concepts to non-technical stakeholders.
Certifications:
- Consider obtaining certifications like SAS Certified Clinical Trials Programmer or Certified Clinical Data Manager (CCDM) to validate your skills.
Internships and Experience:
- Seek internships or entry-level positions in clinical research, pharmaceutical companies, or healthcare institutions to gain practical experience.
Networking:
- Build a professional network by attending conferences, joining industry associations, and connecting with peers and mentors.
Continuous Learning:
- Stay updated with the latest developments in clinical research, statistical methodologies, and regulatory changes through ongoing education and professional development.
Soft Skills:
- Hone soft skills like problem-solving, attention to detail, and adaptability to excel in this role.

By following these steps and continually enhancing your skills and knowledge, you can embark on a rewarding career as a clinical statistician and programmer, contributing to important healthcare research and drug development initiatives.

What skills help clinical statisticians and programmers find jobs?

Clinical statisticians and programmers can improve their job prospects by possessing a combination of technical, analytical, and soft skills. Here are the skills that can help them find jobs:

Statistical Analysis: Proficiency in advanced statistical methods and data analysis techniques used in clinical research
Statistical Software: Expertise in statistical software tools such as SAS, R, or Python for data analysis and modeling.
Clinical Knowledge: Understanding of clinical trial design, drug development processes, and relevant regulatory guidelines
Data Management: Skills in data cleaning, transformation, and database management to ensure data accuracy and integrity
Programming: Ability to write and optimize code for data manipulation, analysis, and reporting.
Clinical Data Analysis: Experience in analyzing clinical trial data, including safety and efficacy assessments.
Regulatory Compliance: Knowledge of regulatory requirements, such as Good Clinical Practice (GCP) and FDA guidelines, for conducting clinical trials.
Effective Communication: Strong communication skills to collaborate with cross-functional teams and convey statistical findings to non-technical stakeholders.
Problem-Solving: Critical thinking and problem-solving abilities to address data anomalies and research challenges.
Attention to Detail: Precision in data analysis and documentation to ensure high-quality results.
Soft Skills: Effective time management, teamwork, and adaptability to work efficiently in a fast-paced environment.
Certifications: Obtaining relevant certifications, such as SAS Certified Clinical Trials Programmer or Certified Clinical Data Manager (CCDM), can validate your skills.
Clinical Trial Software: Familiarity with software used for clinical trial management, electronic data capture (EDC), and regulatory submissions.
Continuous Learning: Staying updated with evolving statistical methodologies, industry trends, and regulatory changes through ongoing education and professional development.
Networking: Building a professional network within the clinical research and pharmaceutical industry can lead to job opportunities and career growth.
Ethical Conduct: Adhering to ethical standards in data handling and research practices.

By combining technical expertise with effective communication and collaboration skills, clinical statisticians and programmers can excel in roles related to clinical research, drug development, and regulatory compliance. Tailoring your skills to match specific job requirements and industry needs is key to success in this field.

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Job ID: 08572
Location: [Hybrid]

Employment Type: Contract

We are seeking an experienced Project Manager to oversee ERP modernization projects that support one of our Delaware based clients. The ideal candidate will have a strong background in the finance and administration of pension plans, pension benefits, and retirement plans.

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