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Director Statistical Programming Jobs in Oneonta, NY

Senior Manufacturing Engineer

Hobart, NY

$94K - $129K/yr

... Director, Technical Services Operations as needed. The Senior Manufacturing Engineer will also ... Complete statistical analysis of data. * Knowledge of DOE, statistical techniques for data analysis ...

Senior Manufacturing Engineer

Hobart, NY · On-site

$94K - $129K/yr

... Director, Technical Services Operations as needed. The Senior Manufacturing Engineer will also ... Complete statistical analysis of data. * Knowledge of DOE, statistical techniques for data analysis ...

Director Statistical Programming information

See Oneonta, NY salary details

$160K

$291.9K

$358.5K

How much do director statistical programming jobs pay per year?

As of Jul 27, 2026, the average yearly pay for director statistical programming in Oneonta, NY is $291,940.00, according to ZipRecruiter salary data. Most workers in this role earn between $271,500.00 and $336,100.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Director of Statistical Programming, and why are they important?

To thrive as a Director of Statistical Programming, you need advanced expertise in statistical analysis, programming languages such as SAS or R, and a strong background in clinical trial data, typically supported by a degree in statistics, mathematics, or a related field. Familiarity with regulatory submission processes, CDISC standards, and project management tools is essential, as are relevant certifications like SAS Certified Professional. Leadership, effective communication, and strategic thinking are key soft skills for managing teams and collaborating across departments. These skills ensure high-quality data outputs, regulatory compliance, and successful execution of complex clinical development projects.

What Is the Job of a Director Statistical Programming?

The job of a director of statistical programming oversees the development and implementation of SAS programs to produce statistical analysis datasets. In this career, your responsibilities include managing the team that generates tables and graphs using the SAS programs for applications such as clinical studies. Other duties include participating in the planning and review of statistical analysis and studying reports, abstracts, and manuscripts as required. You collaborate with project leads to contribute to department operations and standards, such as CDISC for clinical research.

How does a Director of Statistical Programming typically collaborate with cross-functional teams in a pharmaceutical or biotech company?

A Director of Statistical Programming regularly works with biostatistics, clinical data management, regulatory affairs, and medical writing teams to ensure that statistical deliverables meet project timelines and regulatory requirements. They coordinate programming efforts across multiple studies, provide leadership and mentorship to programming staff, and help resolve technical or resource-related challenges. Effective collaboration is essential to streamline workflows, maintain data integrity, and ensure clear communication of statistical results within the organization.

What does a Director of Statistical Programming do?

A Director of Statistical Programming oversees teams responsible for the programming and analysis of clinical trial data, ensuring the accuracy and integrity of statistical outputs. They set departmental strategies, manage resources, and ensure compliance with regulatory requirements and industry standards. This role also involves collaborating with other departments, such as biostatistics and clinical operations, to support the successful delivery of statistical analyses for drug development and regulatory submissions. They play a key leadership role in mentoring staff and advancing programming processes and technologies.
What cities near Oneonta, NY are hiring for Director Statistical Programming jobs? Cities near Oneonta, NY with the most Director Statistical Programming job openings:
Infographic showing various Director Statistical Programming job openings in Oneonta, NY as of July 2026, with employment types broken down into 1% As Needed, 82% Full Time, 13% Part Time, 1% Temporary, and 3% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $291,940 per year, or $140.4 per hour.

$94K - $129K/yr

Full-time

Posted 5 days ago


Job description

Why Us?

At Par Health, we believe great healthcare is built on getting the essentials right. We're looking for passionate, talented individuals who share our commitment to improving lives. With a global workforce, we lead with pride and purpose-prioritizing quality and safety while fostering a culture of continuous improvement, accountability, and teamwork. Elevating the Essentials isn't just our tagline, it's the higher standard we live by every day.

Job Description Summary

Reporting to the Sr Project Mgr - Product Development at the Hobart Site, the Senior Manufacturing Engineer located at the Hobart Site, will work with Product Research and Development (R&D) at the Webster Groves Site to assist in the development, scale-up and transfer of new products to the Hobart site. As products of purchased ANDA's, other Pharma companies and internal R&D are sanctioned the candidate will execute the projects as the Technical Lead. The Senior Manufacturing Engineer will be the subject Matter Expert (SME) for Development, Scale-up, Tech Transfer, Validation and Commercialization of Oral Solid (Tablets and Capsules) and Oral Liquid Dosage Forms. In addition, the Senior Manufacturing Engineer will use problem-solving techniques to support the manufacturing of Legacy Oral Solid (Tablets and Capsules) and Oral Liquid Dosage Forms. Additionally, the candidate will resolve process difficulties, reduce waste, improve productivity and safety, and assist in training and make recommendations to the Director, Technical Services Operations as needed. The Senior Manufacturing Engineer will also provide technical support to site operations, maintenance, and manufacturing personnel for supported processes. The Senior Manufacturing Engineer will have the technical knowledge and skill sets to support all Fluid-bed related activities including developing and manufacturing of Fluid Bed Granulation, Drying and Coating plus Tableting and Encapsulation.

Job Description

Essential Functions

  • Evaluate the feasibility of new products for development and approved ANDA's of other Pharma companies for Tech Transfer and Commercialization.
  • Technically lead the products from development through Commercialization including Validation support.
  • Evaluation of second source API vendors and excipient suppliers.
  • Resolution of Plant CAPA's with Subject Matter Expertise.
  • Evaluation of customer complaints related to physico-chemical characteristics of Dosage Form.
  • Equipment (Fluid Bed Dryer) upgrades.
  • Extension of Product expiry dating.
  • Component changes (bottles/caps) and product monitoring.
  • Product transfers between Tablet presses.
  • New launches.
  • Scale-up and scale-down of current commercial product batch sizes.
  • Use problem solving techniques to resolve manufacturing issues, reduce cost, waste and improve quality with existing processes.
  • Develop/write/execute development protocols for existing products and new product transfers.
  • Support of maintenance and production activities including equipment design/set up, equipment/parts changes, and process modifications.
  • Provide technical leadership in support of productivity improvement and cost reduction projects.
  • Review all process changes to improve products for operation, reliability, efficiency, and safety.
  • Primary resource for resolving technical process issues.
  • Support productivity improvements through process upgrades.
  • Support new process start-ups including equipment and process development.
  • Use knowledge and practical application of materials sciences for solid and liquid dosage formulation characterization and scale-up projects.
  • Manage development activities to ensure projects meet the development schedule requirements. Develop/write product manufacturing instructions.
  • Develop/write product characterization protocols and reports.
  • Complete statistical analysis of data.
  • Knowledge of DOE, statistical techniques for data analysis, total quality management, Six Sigma in manufacturing.
  • Strong communication skills are required to manage projects effectively. This includes the ability to direct and motivate personnel who are not in the same department or function.

Department Specific/ Non-Essential Functions and Skills

Work with Sr Project Mgr - Product Development to develop project scope and cost details for project budget preparation. Regular participation in daily Product and Process Technology meeting. Assist project engineering with installation and startup of process and product upgrade projects. Manage special projects or tasks as assigned.

Minimum Requirements

Education required/ preferred:

MS/Ph.D preferably with related technical background.

Demonstrated ability to troubleshoot pharmaceutical operating equipment and support equipment. Pharmaceutical Formulation experience and or scale-up experience with solid and liquid dosage formulations. Preferred candidate to have minimum 3 - 5 years of experience.

Experience:

This job requires strong written and verbal communication to include technical communication skills, to accurately convey technical issues and information. Understanding of solid and liquid pharmaceutical formulations and hands on experience in the manufacture of pharmaceutical products.

Preferred Skills/Qualifications:

Strong technical and mathematical aptitude.

Skills/Competencies:

Strong computer literacy-MS office products, statistical analysis (Minitab) and database usage.

Organizational Relationship/Scope:

This position requires interaction with various internal and external department heads, supervisors, and operators to coordinate Product and Process Transfers.

WORKING CONDITIONS:

55% of time will be spent in the office, 45% of time on the production floor. There may also be potential opportunities for trave

Disclaimer:

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position.

The expected base pay range for this position is $78,000- $121,000. Please note that base pay offered may vary depending on factors including job-related knowledge, skills, and experience.

This position is eligible for a bonus in accordance with the terms of the applicable program. Bonuses are awarded at the Company's discretion.

EEO Statement:

We comply with all applicable federal, state, and local laws prohibiting discrimination and harassment, and provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status, or genetic information, or any other classification protected by federal, state or local law. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.