ZipRecruiter

Log In

1

Internship Medidata Rave Programmer Jobs (NOW HIRING)

SystImmune, Inc

Clinical Data Associate

Redmond, WA · On-site

$75K - $95K/yr

... internship or co-op experience in a clinical or pharma setting will be considered. * Exposure to a Clinical EDC system (e.g., Medidata Rave, Veeva EDC) preferred. * SAS, Python, and R programming ...

Kite Pharma

OR · On-site

High School degree and 9+ years of experience in Clinical Programming Preferred Qualifications * 3+ years of experience with Medidata RAVE including database build, edit check programming, data ...

Rho Inc

Clinical Data Manager

... programmers, and clinical operations personnel. You will also independently perform and oversee ... Medidata Rave build certification a plus. * Working knowledge of an electronic data capture (EDC ...

WONESE

Systems Data Analyst

Manhattan, NY · On-site

Proficient experience using multiple languages/platforms for programming including Java R ... Coding, Medidata RAVE, IRT, RBM, PACE, Pinnacle 21, MS SharePoint, sFTP with vendors etc. Strong ...

Ōura

Senior Data Engineer

Boston, MA · On-site +1

$115K - $156K/yr

Medidata Rave, Castor, REDCap) and data engineering tools (e.g. AWS S3, Glue, Athena; Databricks; Dagster; dbt) * Experience bridging clinical data management and research with enterprise practices ...

Alnylam

Senior Clinical Data Manager

Cambridge, MA · On-site

$131K - $178K/yr

Collaborate with internal and external partners, including Biostatistics, Statistical Programming ... Experience working with Oracle InForm and Medidata Rave * Experience using standardized medical ...

New

Systimmune

Clinical Data Analyst, Spotfire

Redmond, WA · On-site

$90K - $130K/yr

Experience with SAS/R, SQL programming, and data manipulation. * Familiarity with clinical trial ... Experience integrating Spotfire with clinical databases and EDC systems (e.g., Medidata RAVE ...

4D Molecular Therapeutics

Clinical Technology Manager

$110K - $150K/yr

Bachelor's degree in Computer Science, Engineering, Life Sciences, or a related discipline (or ... Experience with Medidata Rave, SAS (Grid, Viya, 9.4), Spotfire, and Veeva TMF and RIM. * Experience ...

Kite Pharma

OR · On-site

In this role you will work closely with the Biostatistics, Programming, and Clinical Operations ... Proficient in web-based Electronic Data Capture (such as Medidata Rave and other clinical data ...

next page

Showing results 1-20

People also search for

All JobsInternship Medidata Rave Programmer Jobs

Internship Medidata Rave Programmer information

See salary details

$12

$39

$68

How much do internship medidata rave programmer jobs pay per hour?

As of Jun 4, 2026, the average hourly pay for internship medidata rave 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 are the key skills and qualifications needed to thrive as an Internship Medidata Rave Programmer, and why are they important?

To thrive as an Internship Medidata Rave Programmer, you need a solid background in computer science or life sciences, familiarity with clinical data management concepts, and basic programming skills. Experience with Medidata Rave EDC platform, clinical trial management systems, and understanding of CDISC standards or certifications like Medidata Rave certification are valuable. Attention to detail, problem-solving abilities, and strong communication skills help you collaborate effectively with clinical teams and ensure data integrity. These skills are essential for supporting efficient, compliant data capture and management in clinical research environments.

What are some typical projects or tasks an Internship Medidata Rave Programmer might work on?

As an Internship Medidata Rave Programmer, you can expect to assist with building and maintaining electronic case report forms (eCRFs), validating study configurations, and supporting data management teams in clinical trials. You may also help troubleshoot and resolve issues within Medidata Rave, perform quality checks, and contribute to documentation. Collaboration with experienced programmers and data managers is common, providing valuable exposure to real-world clinical data workflows and industry best practices.

What does an Internship Medidata Rave Programmer do?

An Internship Medidata Rave Programmer assists in designing, developing, and maintaining electronic data capture (EDC) systems using Medidata Rave for clinical trials. Their main tasks include programming study databases, building case report forms (CRFs), and ensuring data quality and compliance with regulatory standards. Interns typically work under the supervision of experienced programmers and may also help troubleshoot technical issues, support data validation, and learn about clinical data management processes. This role provides hands-on experience with clinical trial technology and helps interns build foundational skills for a future career in clinical data programming.

What is the difference between Internship Medidata Rave Programmer vs Clinical Data Coordinator?

AspectInternship Medidata Rave ProgrammerClinical Data Coordinator
Required CredentialsBasic knowledge of Medidata Rave, relevant coursework or certificationsDegree in life sciences, healthcare, or related field; often additional certifications
Work EnvironmentInternship setting, often in pharmaceutical or biotech companiesClinical trial sites or sponsor organizations, managing data entry and quality
Industry UsageUsed primarily in clinical data management and EDC system setupUsed in clinical trial data collection, management, and compliance

The Internship Medidata Rave Programmer typically focuses on learning and supporting EDC system setup and data management using Medidata Rave, often as part of an internship program. In contrast, a Clinical Data Coordinator manages data collection, quality control, and compliance during clinical trials. Both roles are essential in clinical research but differ in responsibilities and experience levels.

More about Internship Medidata Rave Programmer jobs
What cities are hiring for Internship Medidata Rave Programmer jobs? Cities with the most Internship Medidata Rave Programmer job openings:
What are the most commonly searched types of Medidata Rave Programmer jobs? The most popular types of Medidata Rave Programmer jobs are:
What states have the most Internship Medidata Rave Programmer jobs? States with the most job openings for Internship Medidata Rave Programmer jobs include:
What job categories do people searching Internship Medidata Rave Programmer jobs look for? The top searched job categories for Internship Medidata Rave Programmer jobs are:
Internship Medidata Rave Programmer jobs near you
Infographic showing various Internship Medidata Rave Programmer job openings in the United States as of May 2026, with employment types broken down into 79% Internship, 12% Full Time, 2% Part Time, 6% Contract, and 1% Summer. Highlights an 90% Physical, 4% Hybrid, and 6% Remote job distribution, with an average salary of $82,234 per year, or $39.5 per hour.
Clinical Data Associate

Clinical Data Associate

SystImmune, Inc

Redmond, WA • On-site

$75K - $95K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 29 days ago

Job description

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials. SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discover and IND-enabling stages, representing cutting-edge biologics development. We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
The Clinical Data Associate (CDA) supports the Clinical Data Manager in executing data management activities across clinical trials, with a primary focus on Phase 3 and other large-scale studies. The CDA will gain hands-on experience across the full DM lifecycle while working under the guidance of senior data management staff.
This role is full-time onsite in Redmond, WA. Please note that SystImmune plans to relocate to a new facility in Bothell, WA in the fall.
Responsibilities:
  • Support the CDM in day-to-day data management activities across study start-up, maintenance, and close-out, including tracking open queries and data cleaning timelines.
  • Assist in the development and review of DM documents such as Data Management Plans, CRF Completion Guidelines, and data review plans using established templates and standards.
  • Perform data review activities including query generation, query resolution follow-up, and non-system edit check output review under CDM oversight.
  • Assist with SAE reconciliation and non-CRF data reconciliation activities, escalating issues to the CDM as appropriate.
  • Support medical coding activities using MedDRA and WHO Drug dictionaries, coordinating with the CDM and CRO for medical review.
  • Run and review SAS and/or R programs and data listings as directed; assist in troubleshooting basic programming errors under CDM guidance.
  • Perform UAT (User Acceptance Testing) of EDC systems and edit checks per provided specifications and test scripts.
  • Assist in tracking and coordinating CRO/vendor deliverables, flagging risks or delays to the CDM.
  • Contribute to data quality monitoring by reviewing metrics reports and flagging trends or anomalies to the CDM.
  • Support database lock activities by assisting with lock checklists, outstanding query resolution, and coordination tasks.
  • Participate in the development and review of DM SOPs and process improvement initiatives.
  • All other duties as assigned.

Qualifications:
  • BA or BS in life sciences, health informatics, or a related field.
  • 1-3 years of relevant clinical data management or clinical research experience; equivalent internship or co-op experience in a clinical or pharma setting will be considered.
  • Exposure to a Clinical EDC system (e.g., Medidata Rave, Veeva EDC) preferred.
  • SAS, Python, and R programming knowledge is a plus.
  • Familiarity with CDISC standards (CDASH, SDTM) and GCP guidelines preferred; willingness to develop deep knowledge required.
  • Detail-oriented with strong organizational and time management skills.
  • Effective written and verbal communication skills; ability to work cross-functionally.
  • Eagerness to learn in a fast-paced, clinical-stage biopharmaceutical environment.
  • Oncology experience or interest a plus.

Compensation and Benefits:
The expected base salary range for this position is $75,000 - $95,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate's level qualifications, experience, and skills.
While most offers typically fall within the low to mid-point of the range, we may extend an offer toward the higher end for exceptional candidates whose background and expertise exceeds the requirements of the role.
SystImmune is a leading and well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company's success. SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE.
We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.

Apply