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Computer programming • quincy ma
- Promoted
(Senior) Director, Statistical Programming
Bicara TherapeuticsBoston, Massachusetts, United States- Promoted
Senior Director, Statistical Programming
BioNTech SECambridge, MA, United States- Promoted
Assoc. Producer WBURNews & Programming
Boston StaffingBoston, MA, United StatesComputer Vision Engineer
Merlin LabsBoston, MA, USProgramming Assistant (Therapeutic Activities)
Senior Living ResidencesCanton, Massachusetts, USComputer Repair Technician (40,839+)
Dorchester County Public SchoolsCambridge, Massachusetts, USA- Promoted
Director, Statistical Programming
Seaport TherapeuticsBoston, Massachusetts, United StatesProgramming Project Leader
SanofiCambridge, MA- Promoted
ASSOCIATE PRODUCER, WBUR News and Programming
Inside Higher EdBoston, MA, United StatesManager, Opinion Leader Programming & Commercial Training
Sarepta TherapeuticsCambridge, Massachusetts, USALife Enrichment / Activity Programming Assistant
Charter Senior Living of DedhamDedham, MA2026 Intern, Biostatistics and Programming
ModernaCambridge, Massachusettstutor - Computer Programming
BUKIBoston, MA, US2026 Intern, Biostatistics and Programming
Moderna, Inc.Cambridge, Massachusetts, United StatesAssistant Professor - Computer Science
InsideHigherEdBoston, Massachusetts, United StatesComputer Repair Technician
CellairisBoston, Massachusetts- Promoted
Computer Coach Tutoring Volunteer Opportunity
EthosBoston, MA, United StatesAssistant Professor - Computer Engineering
UMass BostonBoston, Massachusetts, United States- Promoted
Litigation Associate - Computer Hardware & Software
U.S. Bankruptcy Court - District of CTBoston, MA, United States- radiologist (from $ 100,000 to $ 371,475 year)
- engineering director (from $ 177,500 to $ 246,450 year)
- business development manager (from $ 80,000 to $ 240,000 year)
- product management (from $ 190,000 to $ 213,250 year)
- director software engineering (from $ 177,500 to $ 207,500 year)
- associate dentist (from $ 48,000 to $ 200,000 year)
- energy engineer (from $ 139,838 to $ 200,000 year)
- dentist (from $ 50,000 to $ 194,000 year)
- software engineering manager (from $ 157,125 to $ 193,750 year)
- product owner (from $ 133,750 to $ 189,165 year)
- Los Angeles, CA (from $ 53,786 to $ 180,763 year)
- Providence, RI (from $ 86,526 to $ 171,600 year)
- Pompano Beach, FL (from $ 31,200 to $ 135,971 year)
- Long Beach, CA (from $ 31,200 to $ 135,971 year)
- Huntington Beach, CA (from $ 31,200 to $ 135,971 year)
- Coral Springs, FL (from $ 22,800 to $ 135,500 year)
- Austin, TX (from $ 53,625 to $ 135,500 year)
- Virginia Beach, VA (from $ 31,200 to $ 133,799 year)
- St Petersburg, FL (from $ 23,400 to $ 132,600 year)
- St Louis, MO (from $ 23,400 to $ 132,600 year)
The average salary range is between $ 48,417 and $ 106,314 year , with the average salary hovering around $ 61,564 year .
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(Senior) Director, Statistical Programming
Bicara TherapeuticsBoston, Massachusetts, United States- Full-time
Position Overview
Bicara is seeking an experienced (Senior) Director, Statistical Programming to lead the programming function supporting Bicara's oncology clinical programs. This individual will oversee and support statistical and clinical programming activities for all development programs and is responsible for planning, monitoring, organizing and reviewing activities of statistical programming team by working with Biostatistics, Data Management, and other functional stakeholders. The position serves as an in-house expert for statistical programing and data standards, assists the team to develop functional strategies, and drives the development and continuous improvement of procedures, training and standards. The ideal candidate thrives in a dynamic, fast-paced environment and is eager to contribute both technically and strategically to program success. This role is based in our Boston office and follows a hybrid schedule, with three in-office days each week.
Responsibilities
Lead and manage statistical programming activities for clinical studies, ensuring high-quality deliverables and adherence to established timelines. Allocate resources effectively and promote resource sharing across programs to meet organizational goals
Collaborate with biostatisticians, data managers, and cross-functional teams to define programming strategies and requirements, ensuring alignment with overall clinical and regulatory objectives
Develop, validate, and maintain analysis datasets in compliance with CDISC standards, as well as tables, listings, and figures (TLFs) in accordance with regulatory guidelines and internal standards
Review Statistical Analysis Plans (SAPs) to provide feedback, technical input, and strategic recommendations for successful execution
Provide expertise in statistical programming for regulatory submissions (e.g., FDA, EMA, PMDA), ensuring compliance with eCTD and electronic submission standards
Build and maintain software-agnostic solutions and macros to automate repetitive tasks and improve programming efficiency
Manage, mentor, and guide junior programmers, fostering their professional growth and ensuring consistent quality across deliverables
Stay current with industry trends, best practices, and emerging technologies in statistical programming and data analysis to enhance team capabilities and process efficiency
Qualifications
MS degree in Statistics, Computer Science, Mathematics, or a related field
10+ years of progressive statistical programming experience in the pharmaceutical / biotech industry
Oncology drug development experience in programming required, recent oncology experience preferred
Strong and proficient programming skill in SAS and / or R, thorough understanding of ICH Guidelines, relevant regulatory requirements, and CDISC standards
Familiarity with the expectations of regulatory agencies such as the FDA and EMA
Submission experience strongly preferred
Direct experience with NDA / BLA or other regulatory filings, including ISS or ISE
Direct supervisory experience and demonstrated experience in departmental resource allocation preferred
Ability to work effectively and efficiently both independently and as part of a cross-functional team
Strong attention to detail and awareness to elevate issues appropriately
Company Overview
Bicara Therapeutics is a clinical-stage biopharmaceutical company committed to bringing transformative bifunctional therapies to patients with solid tumors. Bicara’slead program,ficerafuspalfa, is a bifunctional antibody that combines two clinically validated targets, an epidermal growth factor receptor (EGFR) directed monoclonal antibody with a domain that binds to human transforming growth factor beta (TGF‑β). Through this dual-targeting mechanism,ficerafuspalfa has the potential to exert potent anti‑tumor activity by simultaneously blocking both cancer cell‑intrinsic EGFR survival and proliferation, as well as the immunosuppressive TGF‑β signaling within the tumor microenvironment. Ficerafuspalfa is being developed in head and neck squamous cell carcinoma, where thereremainsa significant unmet need, as well as other solid tumor types. For more information, please visit www.bicara.com or follow us on LinkedIn or X.
Here at Bicara, we believe in building diverse teams and cultivating a culture where all voices are included. We encourage people from all backgrounds to apply.
Bicara Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.
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