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:

  1. Data Analysis: Analyzing and interpreting clinical trial data to draw meaningful conclusions and insights
  2. Statistical Modeling: Developing and applying statistical models to assess the effectiveness and safety of medical treatments
  3. Data Management: Ensuring the quality and integrity of clinical trial data through data cleaning and validation
  4. Protocol Development: Collaborating with researchers to design statistically sound clinical trial protocols
  5. Regulatory Compliance: Ensuring adherence to regulatory requirements and standards, such as FDA guidelines
  6. Statistical Programming: Writing and implementing code for data analysis and reporting
  7. Safety Monitoring: Monitoring and analyzing adverse events and safety data during clinical trials
  8. Statistical Reporting: Preparing reports, summaries, and documentation for regulatory submissions
  9. Data Visualization: Creating visual representations of data to aid in decision-making and communication
  10. Quality Control: Conducting quality control checks to ensure accuracy and consistency in analysis
  11. Cross-functional collaboration: Collaborating with cross-functional teams, including clinical researchers and data managers
  12. Statistical Consultation: Providing statistical expertise and guidance to support clinical trial design and analysis
  13. Validation and Testing: Validating statistical programs and conducting testing to ensure accuracy
  14. Continuous Learning: Staying updated with industry trends, methodologies, and regulatory changes
  15. 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.

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

Average Base Salary

$84,241

Per Year

$57K$0k

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$0k

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

0%

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:

  1. 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.
  2. Statistical Skills:
    • Develop a strong foundation in statistical concepts, including hypothesis testing, regression analysis, and experimental design.
  3. Programming Proficiency:
    • Learn statistical programming languages such as SAS, R, or Python.
    • Gain expertise in data manipulation and analysis using these languages.
  4. 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.
  5. Data Management:
    • Acquire data management skills to handle and clean clinical trial data effectively.
  6. Statistical Software:
    • Become proficient in using statistical software packages and tools commonly used in clinical research.
  7. Regulatory Compliance:
    • Learn about regulatory guidelines and compliance requirements relevant to clinical trials (e.g., FDA, ICH GCP).
  8. Clinical Data Analysis:
    • Gain experience in analyzing clinical trial data, including safety and efficacy assessments.
  9. Communication Skills:
    • Develop effective communication skills to convey complex statistical concepts to non-technical stakeholders.
  10. Certifications:
    • Consider obtaining certifications like SAS Certified Clinical Trials Programmer or Certified Clinical Data Manager (CCDM) to validate your skills.
  11. Internships and Experience:
    • Seek internships or entry-level positions in clinical research, pharmaceutical companies, or healthcare institutions to gain practical experience.
  12. Networking:
    • Build a professional network by attending conferences, joining industry associations, and connecting with peers and mentors.
  13. Continuous Learning:
    • Stay updated with the latest developments in clinical research, statistical methodologies, and regulatory changes through ongoing education and professional development.
  14. 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:

  1. Statistical Analysis: Proficiency in advanced statistical methods and data analysis techniques used in clinical research
  2. Statistical Software: Expertise in statistical software tools such as SAS, R, or Python for data analysis and modeling.
  3. Clinical Knowledge: Understanding of clinical trial design, drug development processes, and relevant regulatory guidelines
  4. Data Management: Skills in data cleaning, transformation, and database management to ensure data accuracy and integrity
  5. Programming: Ability to write and optimize code for data manipulation, analysis, and reporting.
  6. Clinical Data Analysis: Experience in analyzing clinical trial data, including safety and efficacy assessments.
  7. Regulatory Compliance: Knowledge of regulatory requirements, such as Good Clinical Practice (GCP) and FDA guidelines, for conducting clinical trials.
  8. Effective Communication: Strong communication skills to collaborate with cross-functional teams and convey statistical findings to non-technical stakeholders.
  9. Problem-Solving: Critical thinking and problem-solving abilities to address data anomalies and research challenges.
  10. Attention to Detail: Precision in data analysis and documentation to ensure high-quality results.
  11. Soft Skills: Effective time management, teamwork, and adaptability to work efficiently in a fast-paced environment.
  12. Certifications: Obtaining relevant certifications, such as SAS Certified Clinical Trials Programmer or Certified Clinical Data Manager (CCDM), can validate your skills.
  13. Clinical Trial Software: Familiarity with software used for clinical trial management, electronic data capture (EDC), and regulatory submissions.
  14. Continuous Learning: Staying updated with evolving statistical methodologies, industry trends, and regulatory changes through ongoing education and professional development.
  15. Networking: Building a professional network within the clinical research and pharmaceutical industry can lead to job opportunities and career growth.
  16. 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.


All Jobs: 17

Found Jobs: 17

Showing 1 - 17 | Page 1 of 1
 

MS IT ITSM Developer

Job ID: 7948
Location: Baltimore, MD  [On-Site]
Employment Type: Contract To Hire
The ITSM Developer will work with a team of IT and Healthcare professionals to deliver solutions involving all aspects of service delivery including ITIL Request, Incident, Problem, Change, Knowledge, Asset and other modules designed to automate and add meaningful value to the organization. The ITSM Developer will use software…

Vice President, M/W/DBE Compliance

Job ID: 7946
Location: New York, NY  [Hybrid]
Employment Type: Direct Hire
The client is seeking a Vice President for M/W/DBE Compliance responsible for developing strategy and leading compliance for the Minority and Women Business Enterprise (M/WBE) department. The ideal candidate will have a strong background in M/W/DBE compliance, data analysis, policy development, project management, stakeholder engagement, leadership, and communication. They will…

Network Engineer

Job ID: 7945
Location: Media, PA  [Hybrid]
Employment Type: Contract To Hire
Consultant for Hybrid role in Media PA will design and build a resilient cutting-edge secure network infrastructure. Consultant will be responsible for the design, engineering, deployment, documentation, optimization, and problem management of all enterprise network infrastructure. Duties will include (but are not limited too): Configuration of firewalls and firewall rule sets Work with proxy services,…

Senior Project Manager

Job ID: 7942
Location: Dover, DE  [On-Site]
Employment Type: Contract
The Senior Project Manager (SPM) is responsible for managing, coordinating, and establishing priorities for the complete life-cycle of projects including the planning, design, programming, testing, and implementation of business solutions designed to meet requirements of various departments in the company, such as distribution, finance, and manufacturing. Senior Project Managers are…

Senior Full Stack Java Software Engineer

Job ID: 7939
Location: Wilmington, DE  [Hybrid]
Employment Type: Direct Hire
We are looking for a Senior Full Stack Java Software Engineer for one of our Wilmington based financial services clients. On the Enterprise Application Engineering team, you serve as a member to design and deliver trusted market-leading technology products in a secure, stable, and scalable way. Your extensive technical…

ServiceNow Solutions Engineer

Job ID: 7938
Location: Dover, DE  [Remote]
Employment Type: Contract
We are looking for a ServiceNow Solutions Engineer for a 20-month Remote contract engagement. Candidates should have... • Strong Functional and Technical knowledge of the Platform providing guidance and support to deliver solutions. • Experience in maintaining CMDB, Asset Management and other Asset/Configuration Management repositories. Excellent understanding of Infrastructure configurations, CI classes and their…

Sr Data Engineer

Job ID: 7936
Location: Titusville, NJ  [Remote]
Employment Type: Contract
Sr. Data Engineer Requirements: - Should have 5-8+ Years of IT Experience with Data Engineering and DWH, ETL Data Bases, ETL Pipelines, data migration. - 5-8+ years' experience working with data bases like - Oracle/ SQL, and very strong with SQL Queries. - Should have experience with Python. - Should know some Data…

UI/UX Designer

Job ID: 7935
Location: Dover, DE  [Remote]
Employment Type: Contract
The UI designer will work within the Creative Team and will have a strong collaboration with the Web Team. …

IT Project Manager

Job ID: 7933
Location: Beverly Hills, CA  [On-Site]
Employment Type: Contract
• Define project scope, goals, and deliverables in collaboration with senior management and stakeholders. • Develop full-scale project plans and associated communications documents. …

BA

Job ID: 7930
Location: Berwyn, PA  [Hybrid]
Employment Type: Direct Hire
Confidential posting. Please contact PSCI for more details.…

Data Engineer

Job ID: 7912
Location: Camden, NJ  [Hybrid]
Employment Type: Contract
Overview  PSCI is  seeking a Data Engineer for hybrid work at our client in Camden NJ. This is a 3-6 month contract Bachelor's degree in computer science, information technology, or related field 3+ years of experience in data analytics or business intelligence-related role Experience in analytical or data visualization tools Conceptual knowledge of data and…

Workday Reports Developer

Job ID: 7906
Location: Media, PA  [On-Site]
Employment Type: Direct Hire
Our client is looking for a permanent employee to join their Workday team. The Senior Data Analyst and Report Developer is responsible for partnering with each corporate function and business unit along with our client's HR Systems team to optimize the use of Workday data and applications, specifically through the analytics,…

ENGINEER QA – MP&A

Job ID: 7631
Location: Philadelphia, PA  [Remote]
Employment Type: Direct Hire
Collaborate with business stake holders & product owners to identify, analyze and come up with technical orchestration of business process with the latest tools available.…

Sr Principal Biostatistical Programmer

Job ID: 7249
Location: Wilmington, DE  [On-Site]
Employment Type: Direct Hire
The Sr Principal, Biostatistical Programmer is responsible for processing clinical data required for statistical analysis of Phase I — III clinical trials and leading project teams. Qualifications • BA/BS degree (MS degree in statistics or computer sciences is desired). • Minimum 8 years of programming experience using SAS/Base/Macro/GRAPH in the biopharmaceutical and/or CRO…

Senior Biostatistician to Director, Biostatistics

Job ID: 7248
Location: Wilmington, DE  [On-Site]
Employment Type: Direct Hire
The Senior Biostatistician to Director, Biostatistics is responsible for providing statistical support for drug development programs in all phases of development. Essential Functions of the Job (Key responsibilities) Interact with members of the multidisciplinary project teams to establish project timelines. Provide statistical input to study protocols. Write statistical analysis plans. Monitor internal and…

Lead SAS Programmer

Job ID: 7247
Location: Wilmington, DE  [On-Site]
Employment Type: Direct Hire
The Lead Biostatistical Programmer I is responsible for processing clinical data required for statistical analysis of Phase I — III clinical trials, and leading project teams. Qualifications • Bachelor’s degree in Statistics, Mathematics, Computer Science or health related field. Masters is preferred. • Minimum 5 years of programming experience using SAS Base/Stat/Macro/GRAPH in…

Senior Biostatistician

Job ID: 7246
Location: Wilmington, DE  [On-Site]
Employment Type: Direct Hire
The Senior Manager, Biostatistics to Director, Biostatistics is responsible for providing statistical support to drug development programs. Essential Functions of the Job (Key responsibilities) • Interact with members of the multidisciplinary project teams to establish project timelines. • Provide statistical input to…