ZipRecruiter

Log In

2

Work From Home Clinical Programmer Medidata Rave Jobs

ARTBIO

Senior Director, Clinical Operations

Cambridge, MA · On-site +1

Oversee study operational plans and execution from concept through close out and CSR writing ... Experience with study tools, including CTMS, eTMF, Medidata RAVE, and other EDC systems. About Us ...

Apply Early

Allucent

Senior Clinical Programmer I

When you work at Allucent, that means rolling up your sleeves and applying your unique skill set ... Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for ...

next page

Showing results 1-20

All JobsClinical Programmer Medidata Rave JobsWork From Home Clinical Programmer Medidata Rave Jobs

Work From Home Clinical Programmer Medidata Rave information

See salary details

$24

$64

$102

How much do work from home clinical programmer medidata rave jobs pay per hour?

As of Jul 7, 2026, the average hourly pay for work from home clinical programmer medidata rave in the United States is $64.77, according to ZipRecruiter salary data. Most workers in this role earn between $53.61 and $73.32 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Work From Home Clinical Programmer using Medidata Rave, and why are they important?

To thrive as a Work From Home Clinical Programmer specializing in Medidata Rave, you need a solid background in clinical data management, programming (such as SQL, SAS, or R), and a degree in life sciences or a related field. Familiarity with Medidata Rave EDC, CDISC standards (SDTM, CDASH), and certifications like Medidata Rave Certified Study Builder are often required. Strong attention to detail, problem-solving abilities, and effective remote communication are vital soft skills for excelling in this role. These competencies ensure accurate data capture, regulatory compliance, and seamless collaboration across globally distributed clinical research teams.

How does a work-from-home Clinical Programmer using Medidata Rave typically collaborate with study teams and resolve data management issues remotely?

As a remote Clinical Programmer specializing in Medidata Rave, you will frequently interact with data managers, clinical research associates, and biostatisticians through virtual meetings and collaboration tools. You'll be responsible for programming study databases, building and validating electronic case report forms (eCRFs), and troubleshooting data discrepancies. Effective communication and proactive problem-solving are key, as you may need to quickly address queries or implement changes based on feedback. Most organizations use platforms like Microsoft Teams, Slack, or email to facilitate real-time collaboration, ensuring that despite working remotely, you remain integrated with the wider study team.

What is a Work From Home Clinical Programmer Medidata Rave?

A Work From Home Clinical Programmer Medidata Rave is a professional who remotely designs, builds, and manages electronic data capture systems for clinical trials using Medidata Rave software. They are responsible for creating study databases, programming edit checks, and ensuring data integrity and regulatory compliance. These programmers work closely with clinical teams to support the collection, analysis, and reporting of clinical trial data, all while working from a remote location. Their expertise in Medidata Rave and clinical data management is essential for the successful execution of clinical studies.

What is the difference between Work From Home Clinical Programmer Medidata Rave vs Work From Home Clinical Data Coordinator?

AspectWork From Home Clinical Programmer Medidata RaveWork From Home Clinical Data Coordinator
Required CredentialsBachelor's in Life Sciences, Clinical Data Management, or related field; experience with Medidata RaveBachelor's in Life Sciences, Clinical Data Management; some roles may require certification
Work EnvironmentRemote, primarily using Medidata Rave for data entry and managementRemote or hybrid, managing data entry, cleaning, and query resolution
Employer & Industry UsagePharmaceuticals, CROs, biotech firms using Medidata RavePharmaceuticals, CROs, clinical research organizations

While both roles involve clinical data management, the Clinical Programmer focuses on configuring and programming data capture in Medidata Rave, whereas the Data Coordinator handles data entry, cleaning, and query resolution. Both roles are often remote and require similar educational backgrounds, but their specific responsibilities and tools differ.

What cities are hiring for Work From Home Clinical Programmer Medidata Rave jobs? Cities with the most Work From Home Clinical Programmer Medidata Rave job openings:
What states have the most Work From Home Clinical Programmer Medidata Rave jobs? States with the most job openings for Work From Home Clinical Programmer Medidata Rave jobs include:
What job categories do people searching Work From Home Clinical Programmer Medidata Rave jobs look for? The top searched job categories for Work From Home Clinical Programmer Medidata Rave jobs are:
Work From Home Clinical Programmer Medidata Rave jobs near you
Infographic showing various Work From Home Clinical Programmer Medidata Rave job openings in the United States as of July 2026, with employment types broken down into 68% Full Time, 21% Part Time, and 11% Contract. Highlights an 100% Remote job distribution, with an average salary of $134,731 per year, or $64.8 per hour.
Director, Clinical Data Management

Director, Clinical Data Management

Alnylam Pharmaceuticals

Cambridge, MA • On-site, Remote

$197K - $266K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 15 days ago

Job description

Summary
The Director, Clinical Data Management is responsible for the oversight of data management activities in support of Alnylam studies across all stages of clinical drug development. This position reports to the head of the Clinical Data & Insights group.
Responsibilities:
  • Direct and grow internal data management expertise area, including management of direct reports;
  • Direct and establish standards for data management CRO outsourcing strategy and deliverables, including the CRO selection process and the governance of CRO performance;
  • Oversee the successful execution of all data management activities in support of Alnylam clinical studies in partnership with CROs, including eCRF development, database build, data collection, data coding, cleaning, database lock and archiving;
  • Supervise the execution of cross-functional, internal data review plans by direct reports across all Alnylam clinical studies;
  • Partner with internal and external partners, including Biostatistics, Statistical Programming, Clinical Operations, Medical, Quality Assurance, Clinical Pharmacology and Pharmacometrics, Bioanalytical, Safety & Risk Management (SRM) and Regulatory Affairs; CROs, central and local laboratories, and other vendors;
  • Lead development and implementation of data collection standards, consistent with industry best practice;
  • Lead data management contributions to the development of clinical protocols, clinical study reports and other regulatory documents, e.g. DSURs, Briefing Documents, etc.
  • Oversee development of department workflows, and infrastructure strategy and implementation, such as preferred provider initiatives, SOPs, and templates;
  • Collaborate with Statistical Programming and external vendors to ensure compliance of SDTM clinical datasets, consistent with CDISC standards;
  • Collaborate with Clinical Operations and Quality Assurance to certify the integrity and traceability of all clinical data sources, compliant with 21 CFR Part 11 standards;
  • Direct Data Management GCP inspection readiness efforts; function as a leader for Data Management in GCP inspections;
  • Represent Data Management at internal cross-functional meetings and external vendor leadership meetings;
  • Demonstrate clear alignment with Alnylam Core Values including, Commitment to People, Fiercely Innovative, Purposeful Urgency, Open Culture and Passion for Excellence.

Requirements
  • BS/BA in scientific discipline, MS or equivalent preferred, with at least 15 years of clinical data management experience in a pharmaceutical/biologics/biotechnology company, with at least 5 years in a leadership capacity;
  • Extensive experience managing global studies utilizing an outsourced CDM model from start-up through close-out;
  • Extensive experience managing direct reports and providing performance reviews and career development guidance;
  • Understanding of ICH GCP as well as general knowledge of industry practices and standards;
  • Knowledge and understanding of regulatory requirements and expectations for clinical data systems including 21 CFR Part 11;
  • Expert knowledge of eClinical processes, efficient design/build of an EDC data management system and other Clinical Trial data/Data Management Systems;
  • Expert knowledge and understanding of regulations and industry-adopted data standards, such as CDISC-SDTM and CDASH;
  • Experience using standardized medical terminology, including MedDRA and WHODrug;
  • Experience working with Medidata Rave EDC systems;
  • Experience working with elluminate or other data visualization systems a plus
  • Experience working with MS Office Suite (Excel, Word and PowerPoint) familiar with MS Project;
  • Excellent written and oral communication skills;
  • Highly motivated and flexible, with excellent organizational skills;
  • Ability to work independently and as part of a multi-disciplinary team.

#LI-AB1 #LI-Virtual
U.S. Pay Range
$197,200.00 - $266,800.00
The pay range reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on a number of factors including, but not limited to, relevant experience, skills, and education. This role is eligible for an annual short-term incentive award (e.g., bonus or sales incentive) and an annual long-term incentive award (e.g., equity).
Alnylam's robust Total Rewards package is designed to support your overall health and well-being. We offer comprehensive benefits including medical, dental, and vision coverage, life and disability insurance, a lifestyle reimbursement program, flexible spending and health savings accounts and a 401(k)with a generous company match. Eligible employees enjoy paid time off, wellness days, holidays, and two company-wide recharge breaks. We also offer generous family resources and leave. Our commitment to your well-being reflects our belief that caring for our people fuels the impact we create together.
Learn more about these and additional benefits offered by Alnylam by visiting the Benefits section of the Careers website: https://www.alnylam.com/careers
About Alnylam
We are the leader in RNAi therapeutics - a revolutionary approach with the potential to transform the lives of people with rare and common diseases. Built on Nobel Prize-winning science, Alnylam has delivered the breakthroughs that made RNAi therapeutics possible and are just at the beginning of what's possible. Our deep pipeline, late-stage programs, and bold vision reflect our core values: fierce innovation, passion for excellence, purposeful urgency, open culture and commitment to people. We're proud to be a globally recognized top employer, where an authentic, inclusive culture and breakthrough thinking fuel one another.
At Alnylam, we commit to an inclusive recruitment process and equal employment opportunity. Qualified applicants will receive consideration for employment without regard to their sex, gender or gender identity, sexual orientation, race, color, ethnicity, national origin, ancestry, citizenship, religion, creed, physical or mental disability, pregnancy status or related conditions, genetic information, veteran or military status, marital or familial status, political affiliation, age, or any other factor protected by federal, state, or local law. Alnylam is an E-Verify Employer.

Apply