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Contract Sdtm Programmer Jobs (NOW HIRING)

RTI International

... engineering, and other technical disciplines to solve the world's most challenging problems.We ... The Sr. Stat serves as the primary liaison between internal teams, contract research organizations ...

Sonsoft Inc

MS Data Integration

New York, NY · On-site

SDTM. * Proven experience in development and implementation of clinical standards in a global ... Additional Information Note:- This is a Contract job opportunity for you. Only Only US Citizen ...

Sonsoft Inc

MS Data Integration

New York, NY · On-site

SDTM. * Proven experience in development and implementation of clinical standards in a global ... Additional Information Note:- This is a Contract job opportunity for you. Only Only US Citizen ...

Exelixis

Executive Director, Biostatistics

Alameda, CA · On-site

... Contract Research Organizations for biostatistics, programming, and data management activities ... Developed/reviewed SDTM/ADaM specifications. * Excellent knowledge of FDA/EU/ICH statistical ...

Everest Clinical Research

Senior Biostatistician

$130K/yr

Everest Clinical Research ("Everest") is a full-service contract research organization (CRO ... Programming: * Develop and/or review ADaM dataset specifications. Review and provide input to SDTM ...

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How much do contract sdtm programmer jobs pay per hour?

As of Jun 24, 2026, the average hourly pay for contract sdtm programmer in the United States is $39.54, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $51.44 per hour, depending on experience, location, and employer.

What is the difference between Contract Sdtm Programmer vs Clinical Data Coordinator?

AspectContract Sdtm ProgrammerClinical Data Coordinator
CredentialsTypically requires a degree in life sciences or related field, with experience in SDTM and programming languages like SASUsually requires a degree in health sciences, nursing, or related fields, with knowledge of data management
Work EnvironmentContract-based, often remote or on-site at pharmaceutical or CRO companiesFull-time, on-site or remote, working within clinical trial teams
Industry UsageCommonly used in clinical research, pharmaceutical, and CRO settingsUsed in clinical research organizations, hospitals, and pharmaceutical companies

The Contract Sdtm Programmer focuses on programming and data standards for clinical trial data, while the Clinical Data Coordinator manages data collection, entry, and quality. Both roles are essential in clinical research but differ in technical focus and responsibilities.

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Contract Sdtm Programmer jobs near you
Infographic showing various Contract Sdtm Programmer job openings in the United States as of June 2026, with employment types broken down into 50% Part Time, 2% Temporary, and 48% Contract. Highlights an 80% Physical, 2% Hybrid, and 18% Remote job distribution, with an average salary of $82,234 per year, or $39.5 per hour.

Associate Director, Statistical Programming

Kailera Therapeutics, Inc.

Waltham, MA • On-site

$159K - $195K/yr

Full-time

Medical, Life, Retirement

Posted 4 hours ago

Job description

At Kailera, we are bold, authentic and committed to our mission of developing therapies that give people the power to transform their lives and elevate their overall health. Rooted in an entrepreneurial spirit and a team-oriented culture, we are working together to advance Kailera's mission to advance novel therapies for obesity and related conditions.
We are passionate about creating an inclusive workplace that promotes collaboration, integrity, and excellence. As we expand, we seek the most talented individuals with diverse backgrounds, cultures, perspectives, and experiences to join our team.
What You'll Do:
We are seeking an experienced programmer to join us as Associate Director, Statistical Programming. This is a critical role responsible for leading statistical programming activities on the assigned disease area(s). This role will support clinical trials, regulatory submissions, and other key initiatives.
Required location: Waltham, MA (hub-based, onsite 3-4 days per week)
Responsibilities:
  • Lead statistical programming efforts for clinical studies, including the development and review of programming specifications to ensure clarity, integrity, and compliance with internal and external standards
  • Lead the execution of ad-hoc and post-hoc analyses to support emerging clinical questions, publications, and internal decision-making
  • Oversee and coordinate activities with Contract Research Organizations (CROs), focusing on the implementation of CDISC standards, creation of SDTM, ADaM datasets, and TFLs, and ensuring high-quality deliverables
  • Conduct independent validation and quality checks of statistical programming deliverables from CROs
  • Collaborate closely with statisticians and cross-functional study teams to deliver results in a timely and accurate manner
  • Manage multiple projects simultaneously, ensuring tasks are prioritized effectively to meet deadlines

Required Qualifications:
  • Proven hands-on experience in programming for clinical development, preferably in a leadership role, with a strong preference for late-phase clinical trial support
  • Experience in regulatory submissions, including NDAs, BLAs, and other filings, with experience in ISS/ISE highly desirable
  • Expertise in SAS programming and comprehensive knowledge of CDISC standards
  • Familiarity with ICH/GCP guidelines and global regulatory submission requirements (e.g., FDA, EMA)
  • Extensive experience overseeing CROs, including independent validation of datasets and statistical deliverables

Preferred Qualifications:
  • Background in cardiometabolic diseases or related therapeutic areas is preferred

Education:
  • Advanced degree (MS/PhD) in Biostatistics, Statistics, or a related field
    • MS: Minimum of 8+ years of relevant experience
    • PhD: Minimum of 6+ years of relevant experience

Salary Range
$159,000-$195,000 USD
For Full Time Roles: This range represents the company's good-faith estimate of the salary at the time of posting. Actual pay may vary based on experience, skills, qualifications, location, and internal equity. We also offer comprehensive health coverage, flexible time off, paid holidays, and a year-end shutdown. Enjoy a monthly wellness stipend, generous 401(k) match, tuition reimbursement, commuter benefits, disability and life insurance, plus annual bonus opportunities and equity grants-because your well-being and future matter to us.
EQUAL EMPLOYMENT OPPORTUNITY INFORMATION:
Kailera Therapeutics, Inc. is an Equal Opportunity Employer that does not discriminate on the basis of actual or perceived race (including traits historically associated with race, such as hair texture and protective hairstyles), color, creed, religion (including religious dress and grooming practices), national origin, ancestry, citizenship status, age (40 and over), sex or gender (including pregnancy, childbirth, pregnancy-related conditions, and lactation), gender identity or expression (including transgender status), sexual orientation, marital status, military service and veteran status, physical or mental disability, genetic information, reproductive health decisions, domestic victim status, political affiliation, or any other characteristic protected by applicable federal, state, or local laws and ordinances.
E-Verify:
Kailera Therapeutics, Inc. uses E-Verify to confirm the identity and employment eligibility of all new hires.
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