Top 23 Sas programmer Jobs in Waltham Ma

Part-Time Contract Statistical Programmer
Keros Therapeutics —Lexington, MA
- $114 - $133 an hour
- Part-time
- Remote
- Computer Science
- 8 years
- Senior level
Statistical Programmer
Rhythm Pharmaceuticals —Boston, MA
- $110,000 - $165,000 a year
- Full-time
- Computer Science
- Office
- SQL
Sr. Statistical Programmer – Level 1
Clymb Clinical —Burlington, MA
- Full-time
- Computer Science
- Mid-level
- Office
Associate Director, Statistical Programming
Alkermes, Inc. —Waltham, MA
- Full-time
- Hybrid work
- Psychiatry
- Office
- Master's degree
Lead Statistical Programmer
Katalyst Healthcares & Life Sciences —Boston, MA
- Contract
- Hybrid work
- Business development
- Analysis skills
- Presentation skills
Quick Apply
Principal Biostatistician (FTE or Contract)
eClinical Solutions —Mansfield, MA
- $175,000 - $215,000 a year
- Full-time
- Remote
- English
- Master's degree
- Analysis skills
Quick Apply
4d
Senior Manager, Statistical Programming
Servier —Boston, MA
- $151,000 - $172,000 a year
- Full-time
- 5 years
- Team management
- Quality control
- Disability insurance
- Health insurance
Associate Director, Biostatistics
Rhythm Pharmaceuticals —Boston, MA
- $160,000 - $240,000 a year
- Full-time
- 5 years
- Office
- Analysis skills
1d
Associate Director, Statistical Programming
Servier —Boston, MA
- $165,000 - $200,000 a year
- Full-time
- 8 years
- Travel
- Mentoring
- Disability insurance
- Health insurance
Director, Biostatistics
Treeline Biosciences —Watertown, MA
- $226,425 - $257,000 a year
- Office
- 3 years
- Doctor of Philosophy
Quick Apply
Principal Statistical Programmer
Vertex Pharmaceuticals —Boston, MA
- $149,200 - $223,800 a year
- Full-time
- Bachelor of Science
- Writing skills
- 8 years
- Loan repayment program
- Health insurance
Senior Director, Biostatistics
Rhythm Pharmaceuticals —Boston, MA
- $210,000 - $300,000 a year
- Full-time
- Office
- Doctor of Philosophy
- Quality control
2d
Clinical Trials Project Manager Senior
Mass General Brigham Incorporated —Boston, MA
- $78,936.00 - $128,928.80 a year
- Full-time
- Hybrid work
- 3 years
- Bachelor's degree
- Neurology
- Opportunities for advancement
Quick Apply
8d
Associate Director of Statistical Programming
Harvard University —Boston, MA
- Full-time
- Hybrid work
- Computer science
- Computer Science
- Master's degree
- Commuter assistance
- Health insurance
1d
Director, Biostatistics
Monte Rosa Therapeutics, Inc —Boston, MA
- $230,000 - $265,000 a year
- Full-time
- Computer science
- Management
- Computer Science
Senior Director, Statistical Programming
Bicycle Therapeutics —Lexington, MA
- $215,000 - $270,000 a year
- Full-time
- Hybrid work
- Office
- Mentoring
- Senior level
- Health insurance
- Dental insurance
Quick Apply
Executive Director, Biostatistics
Sarepta Therapeutics —Cambridge, MA
- $256,000 - $320,000 a year
- Full-time
- Hybrid work
- 11+ years
- Master's degree
- Analysis skills
Sr. Manager, Statistics
Takeda Pharmaceutical —Boston, MA
- $137,000 - $215,270 a year
- Online Application
- Management
- Math
- Doctor of Philosophy
- Paid holidays
- Disability insurance
1d
Principal ADS Program Lead
Genentech —Boston, MA
- $136,400 - $253,200 a year
- Online Application
- 6 years
- Computer Science
- Writing skills
Analytics CoE Senior Manager
Vertex Pharmaceuticals —Boston, MA
- $144,000 - $216,000 a year
- Full-time
- Hybrid work
- Doctoral degree
- Master's degree
- Senior level
- Loan repayment program
- Health insurance

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sas programmer jobs near waltham ma

Part-Time Contract Statistical Programmer

Keros Therapeutics -
Lexington, MA

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Job Details

Part-time | Contract
$114 - $133 an hour

Qualifications

FDA submissions
Biostatistics-based research
Procedural guides
SAS
Team leadership
SAS language
CDISC standards
Managing clinical research teams
System development
Regulatory submission editing and review
Communication with regulatory authorities for clinical trials
Standard operating procedures (SOPs)
General management

Full Job Description

At Keros, our mission is to deliver significant clinical benefit to a wide range of patients with disorders that are linked to dysfunctional signaling of the transforming growth factor-beta (TGF-ß) family of proteins. With a focus on developing differentiated product candidates that are designed to alter TGF-β signaling, we aim to target the pathways critical for the growth, repair and maintenance of blood cells and a number of tissues, including bone, skeletal muscle, adipose and heart tissue. We believe our product candidates have the potential to unlock the full therapeutic benefits of modulating the TGF-β superfamily and provide disease-modifying benefit to patients.

Job Summary:

Provide statistical and clinical programming expertise cross-functionally with the clinical study team. This individual will be responsible for the oversight and execution of statistical and clinical programming activities in Keros's clinical development programs. This position will report to the head of Biometrics.

Primary Responsibilities:

Design/Establish SAS program library for clinical trial reporting, data review tools, and statistical analyses.
Work with the clinical study team to draft and finalize custom report programming specifications required for data listings, patient profiles, data displays and metrics reporting.
Develop SAS programs and macros per report programming specifications and perform hands-on SAS programming support as required.
Support and review clinical data management study documents including Case Report Forms (CRFs), Data Management Plan (DMP), Database Specifications, Electronic Edit Checks, Manual Data Listings Review Plan and Data Transfer Specifications in CDISC format as it relates to the data management functional area.
Identify and drive opportunities to continuously enhance statistical programming processes, SOPs, and technologies.
Provides comprehensive programming leadership and strategy across multiple clinical programs and therapeutic areas as needed.
Lead programming activities in regulatory filings, including the submission of eCTD of BLA/NDA to FDA and other regulatory agencies.
Oversee the activities of CRO programming team to ensure deliverables are in accordance with service agreements, study milestones/timelines and with quality.
Oversee/Perform programming activities for SDTM datasets, ADaM datasets, TFLs for CSR, publications, data review, and ad hoc analysis.
Author/Review data specifications for SDTM and ADaM datasets as well as define.xml files, reviewers guide documents and Pinnacle 21 validation reports.
Participate in team/vendor meetings and study document reviews, e.g. clinical study protocols, eCRF, data transfer specifications, SAP and mock TFL shells.
Monitor data integrity throughout study execution by partnering with Biostatistics, Data Management, Clinical Development Operation and Clinical Science.

Qualifications:

Graduate degree in Biostatistics/Statistics, Computer Science or a related field with 8+ years of statistical programming experience in the pharmaceutical / CRO industry
3+ years of overseeing technical professionals in a regulated environment
Experience building in-house statistical computing environment, SOPs and processes
Strong hands-on SAS programming skills on both clinical trial reporting and system macro development. General knowledge of R is a plus
Expert knowledge with CDISC standards for SDTM and ADaM and statistical programming requirements for regulatory submissions
Recent experience with BLA/NDA or other regulatory filing, including ISS or ISE. Oncology experience is a plus
Global clinical trial and CRO management experience
Excellent written and verbal communication skills
Team player who embraces culture and pace in a startup company

Attributes:

Ability to evaluate, propose and implement creative approaches
Ability to work effectively with minimal structure as well as determine when structure is needed and develop related procedures
Effective communication skills to convey programming considerations
Able to manage multiple projects simultaneously, to manage conflicting priorities, and to be flexible when priorities change

Our Diversity, Equity & Inclusion Mission Statement: Keros is an inclusive company. We believe that diversity drives innovation. We continue to build an inclusive culture that encourages, supports, and celebrates the diverse voices of our employees. As such, Keros takes a holistic approach in mentoring, coaching, and developing all of our Keros team members.

Keros Therapeutics is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected veteran status, or any other characteristic protected by applicable federal, state, or local law.

Recruitment & Staffing Agencies:
Keros Therapeutics does not accept unsolicited resumes from any source other than the candidate directly. Any unsolicited submission by an agency to Keros is prohibited. Any resume submitted by an agency without a signed contract or expressed consent by a member of the Keros Therapeutics Human Resources Department, will be considered property of Keros Therapeutics, and no fee shall be owed with respect thereto.

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sas programmer jobs in waltham ma

Part-Time Contract Statistical Programmer

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Principal Biostatistician (FTE or Contract)

Senior Manager, Statistical Programming

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Principal Statistical Programmer

Senior Director, Biostatistics

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Senior Director, Statistical Programming

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Sr. Manager, Statistics

Principal ADS Program Lead

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