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Trainee Medidata Rave Programmer Jobs (NOW HIRING)

FUTRUE

$79.65 - $113.79/hr

... Programmierung, Durchführung und Dokumentation von User-Acceptance-Tests sowie die Freigabe von ... EDC-Systeme wie Medidata Rave, Oracle Clinical, Veeva EDC, Castor EDC oder vergleichbaren ...

New

3ds

Senior Data Scientist

New York, NY · On-site

$114K - $153K/yr

Medidata is powering smarter treatments and healthier people through digital solutions to support ... The AI features developed will power modern clinical trial study design and study conduct with Rave ...

Actalent

Clinical Data Coordinator

New Haven, CT

$28 - $31.83/hr

Experience with Oracle software, Medidata Rave, EPIC, and ONCORE. * Knowledge of federal ... About Actalent Actalent is a global leader in engineering and sciences services and talent ...

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 ...

Actalent

Sr. Clinical Research Coordinator

Bronx, NY · Hybrid

$35 - $42/hr

Knowledge of EDC systems such as Medidata Rave, REDCap, or similar platforms Why Join Us ... About Actalent Actalent is a global leader in engineering and sciences services and talent ...

Systimmune

Clinical Data Manager

Redmond, WA · On-site

$100K - $170K/yr

Experience working within a Clinical EDC system (e.g., Medidata Rave, Veeva EDC). * SAS programming experience. * Experience with managing Lab Data, such as PK, PD, and Biomarkers. * Detail-oriented ...

Agilent

Collaborate with Biostatistics and Programming functions to ensure development of submission-ready ... Demonstrated experience designing and managing studies using EDC platforms such as Medidata Rave ...

SystImmune, Inc

Clinical Data Manager

Redmond, WA · On-site

$100K - $170K/yr

Experience working within a Clinical EDC system (e.g., Medidata Rave, Veeva EDC). * SAS programming experience. * Experience with managing Lab Data, such as PK, PD, and Biomarkers. * Detail-oriented ...

Crio, Inc.

Director of Product

$170K - $200K/yr

Serve as the internal expert on the sponsor EDC landscape (e.g., systems such as Medidata Rave and ... Build and maintain strategic relationships with Engineering, Sales, Marketing, Customer Success ...

Everest Clinical Research

Clinical Database Designer I

$50K - $90K/yr

One year clinical database design experience, such as developing clinical databases in DFdiscover, InForm, Medidata Rave, Clinical One, and/or other EDC systems. * Software programming experience ...

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Trainee Medidata Rave Programmer information

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

As of Aug 21, 2026, the average hourly pay for trainee 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 is the difference between Trainee Medidata Rave Programmer vs Junior Clinical Data Coordinator?

AspectTrainee Medidata Rave ProgrammerJunior Clinical Data Coordinator
Required CredentialsBasic knowledge of Medidata Rave, relevant coursework or certificationsDegree in life sciences or related field, some data management training
Work EnvironmentClinical trial data management teams, often in CROs or pharma companiesClinical trial sites or data management departments within pharma
Industry UsagePrimarily in clinical data management and EDC system setupData collection, validation, and quality control in clinical trials

The Trainee Medidata Rave Programmer focuses on learning and supporting EDC system setup and data entry using Medidata Rave, while the Junior Clinical Data Coordinator handles data validation and management at clinical sites. Both roles require familiarity with clinical data processes but differ in responsibilities and focus areas.

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Trainee Medidata Rave Programmer jobs near you
Infographic showing various Trainee Medidata Rave Programmer job openings in the United States as of August 2026, with employment types broken down into 92% Full Time, and 8% Part Time. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution, with an average salary of $82,234 per year, or $39.5 per hour.

Manager/Senior Manager, Clinical Data Management

Beam Therapeutics

Cambridge, MA • On-site

Full-time

Re-posted 10 days ago

Job description

Company Overview:
Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.
Position Overview:
We are seeking a motivated and experienced Clinical Data Management professional to serve as the sponsor-side data management lead for assigned clinical studies within our growing development portfolio.
Reporting to the Senior Director of Data Management, this role is responsible for driving study-level data management activities from study start-up through database lock while ensuring high-quality, inspection-ready clinical data. The Manager/Senior Manager will work closely with Clinical Operations, Biostatistics, Statistical Programming, Medical, Regulatory, and external partners to support the successful execution of clinical trials.
This role is ideal for an experienced clinical data manager who enjoys hands-on study ownership, cross-functional collaboration, and helping advance innovative therapies in a fast-paced biotechnology environment.
Primary Responsibilities:
Lead Study-Level Data Management Activities
  • Serve as the sponsor-side Clinical Data Management lead for assigned clinical studies.
  • Manage clinical data management activities from study start-up through database lock and archival.
  • Ensure clinical data are complete, accurate, and fit-for-purpose to support study objectives, interim analyses, clinical study reports, and regulatory submissions.
  • Track and communicate study-level data management metrics, risks, and timelines.
  • Drive issue resolution and proactively identify opportunities to improve data quality and operational efficiency.

CRO and Vendor Oversight
  • Serve as the primary data management contact for CROs and external vendors supporting assigned studies.
  • Oversee outsourced data management activities to ensure quality expectations and timelines are met.
  • Review deliverables and provide feedback on data management plans, CRF completion guidelines, edit checks, reconciliation plans, and data transfer specifications.
  • Support oversight of external data sources including central laboratories and specialty vendors.
  • Escalate risks, quality concerns, and timeline impacts with recommended mitigation strategies.

Database and Data Quality Management
  • Lead cross-functional review activities for CRF design and database development and ensure adherence to Beam and/or CDASH/CDISC standards.
  • Review edit check specifications and coordinate user acceptance testing activities.
  • Support development and review of Data Management Plans and other study-level documentation.
  • Ensure appropriate reconciliation activities are conducted, including SAE and external vendor reconciliations.
  • Monitor data cleaning activities and partner with CROs to drive timely query resolution and database readiness.

Inspection Readiness and Cross-Functional Partnership
  • Maintain inspection-ready documentation throughout the study lifecycle.
  • Support internal audits, sponsor inspections, and regulatory inspection readiness activities.
  • Collaborate closely with Clinical Operations, Biostatistics, Statistical Programming, Medical Monitoring, Regulatory Affairs, and Quality.
  • Communicate complex data issues clearly and effectively to study teams and leadership.

Qualifications:
  • BS or MS degree in a scientific, health-related, or technical discipline.
  • 5+ years of clinical data management experience within biotechnology, pharmaceutical, or CRO environments.
  • Experience supporting Phase I-III clinical trials from study start-up through database lock.
  • Working knowledge of CDASH/CDISC standards, GCP/ICH requirements, and applicable regulatory expectations.
  • Strong hands-on experience with EDC systems (e.g., Medidata RAVE, Veeva EDC, Oracle Inform).
  • Experience managing CROs and external data vendors.
  • Familiarity with SDTM concepts and clinical data review processes.
  • Experience with data visualization or reporting tools such as J-Review or similar platforms.
  • Strong analytical, organizational, and problem-solving skills.
  • Ability to manage multiple priorities and meet timelines in a fast-paced environment.
  • Excellent written and verbal communication skills.

Preferred Qualifications:
  • Experience supporting late-stage or registrational clinical studies.
  • Experience in gene editing, cell therapy, rare disease, or other complex development programs.

The salary range below 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 several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data.
Beam Pay Range
$130,000-$190,000 USD

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