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Part Time Sdtm Jobs (NOW HIRING)

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Part Time Sdtm information

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$19

$54

$80

How much do part time sdtm jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for part time sdtm in the United States is $54.04, according to ZipRecruiter salary data. Most workers in this role earn between $41.59 and $68.03 per hour, depending on experience, location, and employer.

What is a part time SDTM?

Part time SDTM jobs involve working with the Study Data Tabulation Model (SDTM) on a part-time basis, typically in the field of clinical data management or clinical research. SDTM is a standard format developed by the Clinical Data Interchange Standards Consortium (CDISC) for organizing and submitting clinical trial data to regulatory agencies. Professionals in these roles may be responsible for mapping clinical data to SDTM standards, data validation, and ensuring compliance with regulatory requirements, while working less than full-time hours. Part time SDTM positions are ideal for individuals seeking flexibility or balancing other commitments.

What are the key skills and qualifications needed to thrive as a part time SDTM specialist?

To thrive as a Part Time SDTM Specialist, a solid background in clinical data management, knowledge of CDISC standards, and familiarity with SDTM mapping are essential, often supported by a degree in life sciences or a related field. Proficiency with SAS programming, clinical trial databases, and relevant data transformation tools is typically required, along with certifications like CDISC or SAS credentials being advantageous. Attention to detail, analytical thinking, and effective communication are key soft skills that help in coordinating with cross-functional teams and ensuring data quality. These skills ensure accurate data standardization, regulatory compliance, and smooth data submissions in clinical research projects.

What are some common challenges faced by part time SDTM specialists, and how can they be addressed?

Part-time SDTM specialists often face the challenge of managing complex data mapping and standardization tasks within limited working hours. Coordination with full-time team members and meeting project deadlines can also be demanding due to reduced availability. To address these challenges, clear communication, well-documented processes, and effective use of data management tools are essential. Establishing regular check-ins and leveraging collaborative platforms can help ensure that part-time contributors stay aligned with project goals and deliverables.

What is the difference between Part Time Sdtm vs Part Time Clinical Data Coordinator?

AspectPart Time SdtmPart Time Clinical Data Coordinator
Required CredentialsTypically a degree in life sciences or related field; familiarity with SDTM standardsSimilar educational background; often requires knowledge of clinical data management
Work EnvironmentPharmaceutical or biotech companies, clinical research organizationsSame as Sdtm, working within clinical trial teams
Employer & Industry UsageUsed in clinical data management for regulatory submissionsInvolved in data collection, validation, and reporting in clinical trials

Part Time Sdtm and Part Time Clinical Data Coordinator roles share similar educational backgrounds and work environments, focusing on clinical data management. The main difference lies in the specific focus: Sdtm specialists primarily handle standard data tabulation formats, while Clinical Data Coordinators oversee broader data collection and validation processes within clinical trials.

What are the most commonly searched types of Sdtm jobs?

The most popular types of Sdtm jobs are:

What job categories do people searching Part Time Sdtm jobs look for?

The top searched job categories for Part Time Sdtm jobs are:

Part Time Sdtm jobs near you
Infographic showing various Part Time Sdtm job openings in the United States as of August 2026, with employment types broken down into 96% Full Time, 1% Part Time, and 3% Contract. Highlights an 80% Physical, 2% Hybrid, and 18% Remote job distribution, with an average salary of $112,399 per year, or $54 per hour.

Part-Time Contract Statistical Programmer

Keros Therapeutics

Lexington, MA • On-site, Remote

$114 - $133/hr

Full-time, Part-time

Re-posted 10 days ago

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

This pay range represents the base hourly rate or base annual full-time salary for all positions in the job grade within which this position falls. The actual base salary offer will depend on a variety of factors including experience, education, and other relevant factors.
Potential base pay range
$114-$133 USD
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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