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Weekend Statistical Programmer Jobs in Virginia (NOW HIRING)

Principal Biostatistician

Triangle, VA · On-site

$125 - $150/hr

S. Food and Drug Administration (FDA) guidance documents pertinent to statistical analysis, pharmacokinetic studies, pharmacokinetic analyses, and reports * Excellent SAS programming skills

Bachelor's or Master's degree in Statistics or related field 5+ years of SAS programming experience in clinical research Experience with CDISC standards Preferred Qualifications: Experience ...

SAS Programmer Location: Remote/Hybrid Job Type: Full-Time Position Overview: Venesco is seeking a ... Collaborate with statisticians and data management teams * Support regulatory submissions and ...

... statisticians and data management teams • Support regulatory submissions and audits Minimum ... programming experience in clinical research • Experience with CDISC standards Preferred ...

Support off‑hours deployment such as evenings or weekends. Qualifications * Must be a U.S ... statistics on applicants. All applicants will receive a decision promptly. We do not discriminate ...

Video Engineer

Virginia Beach, VA · On-site

$50K - $55K/yr

... occasional evening or weekend if required * Ability to communicate effectively and work ... Ability to use standard word processing & spreadsheet software for reports, graphics and statistics

In addition, there may be occasional weekend work required. The candidate MUST be a US citizen and ... Develop and implement statistical models, machine learning workflows, and geospatial analytics ...

Company Description Jr. SAS Programmer Location: Alexandria, VA One year long contract Pay rate: up ... Client will hire an entry level person with a math degree, or statistics, etc. Responsibilities ...

... occasional evening or weekend if required • Ability to communicate effectively and work ... graphics and statistics • Ability to occasionally move equipment, climb ladders, and lift ...

Video Engineer

Virginia Beach, VA · On-site

$50K - $55K/yr

... occasional evening or weekend if required * Ability to communicate effectively and work ... Ability to use standard word processing & spreadsheet software for reports, graphics and statistics

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Weekend Statistical Programmer information

What is the difference between Weekend Statistical Programmer vs Full-Time Statistical Programmer?

AspectWeekend Statistical ProgrammerFull-Time Statistical Programmer
CredentialsBachelor's degree in Biostatistics, Statistics, or related field; often requires programming certificationsSame as weekend role, with additional experience preferred
Work EnvironmentPart-time, flexible hours, often remote or in clinical research settingsFull-time, standard office or remote work in pharmaceutical or biotech companies
Employer & Industry UsageUsed in clinical trials, research organizations, and CROs for flexible staffingCommon in pharmaceutical, biotech, and research institutions for ongoing project support

The main difference between a Weekend Statistical Programmer and a Full-Time Statistical Programmer lies in their work hours and commitment. Weekend roles typically involve part-time, flexible schedules focused on specific project needs, while full-time roles require consistent, ongoing work. Both roles require similar skills and credentials, but the work environment and hours differ to accommodate project demands and work-life balance.

What are the most commonly searched types of Statistical Programmer jobs in Virginia?

The most popular types of Statistical Programmer jobs in Virginia are:

What cities in Virginia are hiring for Weekend Statistical Programmer jobs?

Cities in Virginia with the most Weekend Statistical Programmer job openings:

Principal Biostatistician

Worldwide Clinical Trials

Triangle, VA • On-site, Remote

Full-time

Posted 7 days ago


Job description

Who we are
We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.
Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.
Why Worldwide
We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!
What The Principal Scientist, Biostatistician does at Worldwide
Use independent judgment and technical expertise to assist in designing studies; preparing statistical analysis plans; analyzing data from pharmacokinetic, clinical, and pre-clinical studies; interpreting statistical results from pharmacokinetic, clinical, and related analyses; and generating randomization schedules for clinical studies.
Principal Scientists are recognized as scientific leaders in the company. They regularly contribute to literature and to building Worldwide Clinical Trials' intellectual property and are capable of leading interdisciplinary project teams.
What you will do
  • Accurately and efficiently perform tasks that are broad in scope

  • Use knowledge and judgment to reach well-defined goals in project management

  • Work independently and collaboratively to solve technical problems by implementing contemporary methods

  • Assist the clinic, method development, and marketing/business development by applying knowledge, conducting literature reviews, providing information, and offering related support

  • Train and guide less experienced personnel in techniques required for work assignments

  • Supervise personnel involved in statistical and pharmacokinetic-related work

  • Assist with the design of clinical studies and construct data analysis plans to meet study protocol requirements and maximize information from available data

  • Perform statistical analyses on clinical and pharmacokinetic data using appropriate methods and software programs

  • Prepare documentation for final reports, including text, tables, graphs, and analysis outputs

  • Interact with clients, bioanalytical personnel, and clinical personnel regarding study design, statistical analyses, pharmacokinetic data analyses, and data interpretation

  • Identify problems or potential problems in generating quality statistical and pharmacokinetic documents, report concerns to their supervisor, and propose possible solutions
  • Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.

What your bring to the role
  • Familiarity with corporate policies, goals, and objectives, normally acquired after three months of exposure to Worldwide Clinical Trials' operations

  • Understands and applies Good Laboratory Practice (GLP) guidelines and U.S. Food and Drug Administration (FDA) guidance documents pertinent to statistical analysis, pharmacokinetic studies, pharmacokinetic analyses, and reports

  • Excellent SAS programming skills

  • Proficient in the use of WinNonlin, nQuery, Microsoft Word, and Microsoft Excel

  • Ability to read, write, and understand complex literature

  • Ability to write concise, understandable study reports and communicate clearly with clients and Worldwide Clinical Trials personnel

  • Ability to create, understand, and interpret graphs, tables, and charts

  • Strong organizational and problem-solving skills and ability to set priorities

  • Ability to interact effectively with superiors, peers, and others and communicate ideas clearly

  • Ability to follow and implement Worldwide Clinical Trials' policies and Standard Operating Procedures, normally associated with three months of experience at Worldwide Clinical Trials

Your experience
  • PhD or postgraduate degree with a scientific focus preferred

  • Bachelor's degree with a scientific focus and 12 or more years of relevant work experience required

Promotion to the next level is not automatic based on years of experience. Personnel are evaluated on proven competency, level of responsibility, and ability to work independently.
At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation.
The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):
United States of America - $96,500.00 - $191,500.00
The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.
We love knowing that someone is going to have a better life because of the work we do.
To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.