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Medidata Rave Remote Jobs in Texas (NOW HIRING)

Faeth Therapeutics

Clinical Data Manager

Austin, TX · Remote

$125K - $175K/yr

Remote (U.S.) Responsibilities: * Lead day-to-day data management activities for assigned clinical ... Hands-on experience with EDC systems (e.g., Medidata Rave, Veeva, Oracle InForm) * Strong ...

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Medidata Rave Remote information

What is a Medidata Rave remote?

A Medidata Rave remote job involves working with the Medidata Rave clinical data management system from a location outside of a traditional office, typically from home or another remote setting. Professionals in these roles are responsible for building, managing, or supporting electronic data capture (EDC) systems used in clinical trials. Remote positions can include roles such as database developers, clinical data managers, or support specialists, all of whom collaborate virtually to ensure data integrity and regulatory compliance in clinical research. These jobs require strong familiarity with Medidata Rave software, attention to detail, and effective communication skills for remote teamwork.

What are the key skills and qualifications needed to thrive as a Medidata Rave remote specialist?

To excel as a Medidata Rave Remote Specialist, you need a solid understanding of clinical data management, electronic data capture (EDC) systems, and often a background in life sciences or related fields. Familiarity with the Medidata Rave platform, GCP compliance, and certification in Medidata Rave or similar EDC systems are typically required. Strong analytical thinking, attention to detail, and effective communication skills help professionals manage clinical trial data accurately and collaborate with remote teams. These competencies ensure high-quality data integrity, regulatory compliance, and smooth clinical trial operations in a remote environment.

What are some common challenges faced by remote Medidata Rave professionals, and how can they overcome them?

Remote Medidata Rave professionals often encounter challenges such as coordinating with global clinical teams across time zones and ensuring secure, accurate data entry and management. Communication can be more complex when troubleshooting database issues or implementing protocol amendments from a distance. To overcome these hurdles, it's important to establish clear communication channels, maintain detailed documentation, and participate in regular virtual meetings with study stakeholders. Familiarity with collaborative tools and Medidata Rave's support resources can also help streamline remote workflows and resolve technical issues efficiently.

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

AspectMedidata Rave RemoteClinical Data Coordinator
Required CredentialsExperience with Medidata Rave, clinical data management certificationsDegree in life sciences, training in data management systems
Work EnvironmentRemote, primarily computer-basedOffice or remote, depending on employer
Industry UsageUsed by clinical research organizations and pharma companiesCommonly employed in clinical trial sites and CROs

Medidata Rave Remote specialists focus on managing clinical trial data using Medidata Rave software, often working remotely. Clinical Data Coordinators handle data entry, validation, and management at trial sites or offices. While both roles involve clinical data, Medidata Rave Remote roles require specific software expertise, whereas Clinical Data Coordinators focus on data quality and compliance in clinical settings.

What are popular job titles related to Medidata Rave Remote jobs in Texas?

For Medidata Rave Remote jobs in Texas, the most frequently searched job titles are:

What job categories do people searching Medidata Rave Remote jobs in Texas look for?

The top searched job categories for Medidata Rave Remote jobs in Texas are:

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Medidata Rave Remote jobs near you
Infographic showing various Medidata Rave Remote job openings in Texas as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution.

Clinical Data Manager

Faeth Therapeutics

Austin, TX • Remote

$125K - $175K/yr

Full-time

Medical, Dental, Vision, Retirement

This job post has expired 2 days ago. Applications are no longer accepted.

Job description

Faeth Therapeutics is a clinical-stage oncology company listed on Nasdaq that recently raised $200M in funding. With a strong scientific foundation and a founding team that includes the discoverer of our target pathway, we are advancing PIKTOR, a multi-node PI3K/AKT/mTOR inhibitor program, toward multiple near-term milestones. We are a small, focused team where every person has direct impact - united by a shared commitment to care deeply, create boldly, and never stop learning.

Faeth Therapeutics is seeking an experienced Clinical Data Manager to support clinical data management activities across two active clinical trials. This individual will play a critical role in ensuring high-quality, reliable clinical data through the design, implementation, and oversight of data management processes. The role requires close collaboration with clinical operations, biostatistics, medical, and external vendors.

Reports to: Chief Medical Officer

Location: Remote (U.S.)

Responsibilities:

  • Lead day-to-day data management activities for assigned clinical trials (Phase 2 and Phase 1b)
  • Oversee CRO and vendor data management deliverables to ensure timelines, quality, and compliance
  • Review and contribute to key study documents, including:
  • Data Management Plans (DMPs)
  • Case Report Forms (CRFs) / eCRFs
  • Edit check specifications
  • Data transfer specifications
  • Manage database build, UAT, and database lock activities
  • Ensure data integrity, consistency, and completeness through ongoing data review and cleaning
  • Monitor query generation and resolution timelines
  • Perform data review, listings review, and support medical data review activities
  • Collaborate with biostatistics on data standards (e.g., CDISC/SDTM) and analysis datasets
  • Ensure compliance with GCP, regulatory requirements, and company SOPs
  • Support inspection readiness and participate in audits/inspections as needed
  • Contribute to process improvements and best practices in data management

Requirements:

  • Bachelor's degree in life sciences, computer science, or related field (advanced degree a plus)
  • 5-8 years of clinical data management experience in biotech, pharma, or CRO settings
  • Experience supporting early- to mid-phase clinical trials (Phase 1-2 required)
  • Hands-on experience with EDC systems (e.g., Medidata Rave, Veeva, Oracle InForm)
  • Strong understanding of clinical data standards (CDISC, SDTM)
  • Experience managing CROs and external vendors
  • Familiarity with oncology trials is preferred
  • Knowledge of GCP and regulatory requirements
  • Strong attention to detail and problem-solving skills
  • Excellent communication and cross-functional collaboration skills

Compensation Range: $125,000 - $175,000 (actual compensation may vary based on experience, qualifications and location)

Working at Faeth

Benefits:

  • Competitive salary and equity in a well-funded, clinical-stage biotech
  • 100% remote work and flexible schedule
  • Health, dental, and vision for you and your dependents
  • Flexible time off
  • Generous parental leave
  • Traditional and Roth 401k 
  • Mission oriented, remote first culture

We are an equal opportunity employer, and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

All offers of employment are contingent upon satisfactory completion of a background check and verification of eligibility to work in the United States.

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