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Medidata Rave Jobs in California (NOW HIRING)

IQVIA

Senior Data Team Lead (Remote)

San Francisco, CA · Remote

$86K - $217K/yr

Expertise with Medidata Rave, Oracle InForm, or similar EDC systems. * Strong understanding of GCP, ICH, and clinical research processes. * Excellent communication and leadership skills. * An ...

IQVIA

Senior Data Team Lead (Remote)

San Diego, CA · Remote

$86K - $217K/yr

Expertise with Medidata Rave, Oracle InForm, or similar EDC systems. * Strong understanding of GCP, ICH, and clinical research processes. * Excellent communication and leadership skills. * An ...

IQVIA

Senior Data Team Lead (Remote)

Anaheim, CA · Remote

$86K - $217K/yr

Expertise with Medidata Rave, Oracle InForm, or similar EDC systems. * Strong understanding of GCP, ICH, and clinical research processes. * Excellent communication and leadership skills. * An ...

IQVIA

Senior Data Team Lead (Remote)

Oakland, CA · Remote

$86K - $217K/yr

Expertise with Medidata Rave, Oracle InForm, or similar EDC systems. * Strong understanding of GCP, ICH, and clinical research processes. * Excellent communication and leadership skills. * An ...

IQVIA

Senior Data Team Lead (Remote)

San Diego, CA · Remote

$86K - $217K/yr

Expertise with Medidata Rave, Oracle InForm, or similar EDC systems. * Strong understanding of GCP, ICH, and clinical research processes. * Excellent communication and leadership skills. * An ...

IQVIA

Senior Data Team Lead (Remote)

Anaheim, CA · Remote

$86K - $217K/yr

Expertise with Medidata Rave, Oracle InForm, or similar EDC systems. * Strong understanding of GCP, ICH, and clinical research processes. * Excellent communication and leadership skills. * An ...

IQVIA

Senior Data Team Lead (Remote)

San Francisco, CA · Remote

$86K - $217K/yr

Expertise with Medidata Rave, Oracle InForm, or similar EDC systems. * Strong understanding of GCP, ICH, and clinical research processes. * Excellent communication and leadership skills. * An ...

IQVIA

Senior Data Team Lead (Remote)

Oakland, CA · Remote

$86K - $217K/yr

Expertise with Medidata Rave, Oracle InForm, or similar EDC systems. * Strong understanding of GCP, ICH, and clinical research processes. * Excellent communication and leadership skills. * An ...

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Medidata Rave information

What is a Medidata Rave job?

A Medidata Rave job typically involves working with Medidata Rave, a widely used electronic data capture (EDC) system in clinical trials. Professionals in this role manage study databases, design case report forms (CRFs), ensure data integrity, and support clinical research teams. Roles may include Rave Study Builder, Data Manager, or Clinical Programmer. Strong knowledge of clinical trial processes, database management, and SQL is often required.

What are the key skills and qualifications needed to thrive in the Medidata Rave position, and why are they important?

To thrive as a Medidata Rave specialist, you need a solid understanding of Electronic Data Capture (EDC) systems, clinical data management, and regulatory guidelines, typically supported by certifications in Medidata Rave or relevant clinical research fields. Proficiency with the Medidata Rave platform, user administration, and familiarity with tools such as SQL or other database management systems are highly valued. Strong attention to detail, communication, and problem-solving skills help professionals stand out in this role. These qualities ensure accurate data collection, regulatory compliance, and effective collaboration in complex clinical trial environments.

What are some common challenges faced by Medidata Rave specialists in clinical trials?

Medidata Rave specialists often encounter challenges such as ensuring data accuracy across multiple sites, managing complex study protocols, and troubleshooting technical issues within the platform. They are responsible for configuring case report forms, supporting site users, and maintaining regulatory compliance, which requires constant vigilance and adaptability. Collaboration with clinical research teams, sponsors, and IT staff is vital to address study-specific needs and resolve problems efficiently. These challenges make the role dynamic but also provide opportunities for continuous learning and professional growth.

What are popular job titles related to Medidata Rave jobs in California? For Medidata Rave jobs in California, the most frequently searched job titles are:
What job categories do people searching Medidata Rave jobs in California look for? The top searched job categories for Medidata Rave jobs in California are:
Medidata Rave jobs near you
Clinical Research Data Associate II - The Angeles Clinic & Research Institute

Clinical Research Data Associate II - The Angeles Clinic & Research Institute

Cedars Sinai

Los Angeles, CA • On-site

Other

Posted 25 days ago

Cedars-Sinai rating

8.6

Company rating: 8.6 out of 10

Based on 130 frontline employees who took The Breakroom Quiz

37th of 1,020 rated hospitals

Job description

Why Cedars-Sinai?

At Cedars-Sinai, we pride ourselves on our inclusive and collaborative culture. We are committed to encouraging an environment where diverse perspectives are valued and innovative ideas can flourish. Our team works together to achieve world-class results, and we support each other in reaching our full potential. If you are looking to grow your career in a place that values excellence and impact, Cedars-Sinai is the perfect place for you.

Join us in our mission to transform healthcare and improve patient outcomes. Apply today and become part of a team that is making a real difference in the world!

Grow your career at Cedars-Sinai!

The Angeles Clinic & Research Institute has established an international reputation for developing new cancer therapies, providing the best in experimental and traditional treatments, and expertly guiding and training the next generation of clinicians. Our board-certified fellowship-trained medical oncologists, surgeons, immunotherapists, pathologists, and dermatologists work closely together to advance cancer care. We are committed to bringing innovative therapeutic options to all of our patients with cancer.

Join our team and contribute to groundbreaking research!

The Clinical Research Data Associate II manages the data for assigned research studies. This will include, designing forms for data collection, clinical data abstraction, processing data, maintaining record systems, and producing project reports for studies. In addition, may train clinical research staff, perform basic statistical analysis, and work with bioinformatics to develop and maintain trial management systems. Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board. 

Key Responsibilities:

  • Coordinates data for research studies.
  • Designs forms for data collection.
  • Performs clinical data collection/abstraction.
  • Processes clinical data using a range of computer applications and database systems to support cleaning and management of subject or patient data.
  • Produces project reports.
  • Performs data searches and other related administrative tasks.
  • Participates in required training and education programs.
  • Works closely with study monitors to review study data and respond to inquiries.
  • Provides support and preparation for study audits.
  • May train clinical research staff to help improve the quality of the data being collected.
  • May solve operational/data problems in consultation with other employees and/or supervisors.
  • May perform basic statistical analysis in conjunction with a biostatistician.

Education

  • High School Diploma or GED required
  • Bachelor's degree in a related field (e.g., Life Sciences, Health Sciences, or similar) preferred

Experience

  • Minimum of two (2) years of relevant experience in clinical research or a related setting
  • Hands-on experience with Electronic Data Capture (EDC) systems, preferably within oncology clinical trials
  • Familiarity with EDC platforms such as REDCap, Oracle Clinical, Veeva Vault, Medidata Rave, and/or OpenClinica
  • Proficiency with data management software and related tools
  • Demonstrated ability to work effectively in a collaborative, team-oriented environment
  • Strong attention to detail with excellent organizational and time-management skills
  • Excellent written and verbal communication skills
  • Proven ability to adhere to regulatory requirements and ethical guidelines

Licensure/Certification

  • Certification in Clinical Research (ACRP, SOCRA, or equivalent) preferred

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