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Edc Project Manager Jobs in California (NOW HIRING)

Ardelyx

Clinical Trial Manager

Newark, CA · On-site +1

$136K - $160K/yr

Participate in and support user acceptance testing (UAT) for clinical systems, (e.g., EDC IRT ... Strong project management skills, including managing of timelines, budgets, and cross-functional ...

Ardelyx

Clinical Trial Manager

Newark, CA · On-site +1

$136K - $160K/yr

Participate in and support user acceptance testing (UAT) for clinical systems, (e.g., EDC IRT ... Strong project management skills, including managing of timelines, budgets, and cross-functional ...

Ardelyx

Clinical Trial Manager

Newark, CA · On-site +1

Participate in and support user acceptance testing (UAT) for clinical systems, (e.g., EDC IRT ... Strong project management skills, including managing of timelines, budgets, and cross-functional ...

Ardelyx

Clinical Trial Manager

Newark, CA · On-site +1

$136K - $160K/yr

Participate in and support user acceptance testing (UAT) for clinical systems, (e.g., EDC IRT ... Strong project management skills, including managing of timelines, budgets, and cross-functional ...

Ardelyx

Clinical Trial Manager

Newark, CA · On-site

$136K - $160K/yr

Participate in and support user acceptance testing (UAT) for clinical systems, (e.g., EDC IRT ... Strong project management skills, including managing of timelines, budgets, and cross-functional ...

ImmunityBio

Senior Clinical Data Manager

Culver City, CA · On-site +1

Develop database requirements for use by EDC vendors. Serve as study database manager and work with ... Perform other special projects and duties as requested. Education & Experience * Bachelor's Degree ...

CYNET SYSTEMS

Clinical Data Manager

Sunnyvale, CA · On-site

$70 - $75/hr

Ability of working with multiple teams on multiple projects simultaneously. Desired: * Understand ... efficient EDC design. * Excellent communication skills. * Proficient in MS Office (Excel ...

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Edc Project Manager information

What are some common challenges faced by EDC Project Managers when implementing new electronic data capture systems?

EDC Project Managers often encounter challenges such as ensuring seamless integration of the new system with existing clinical trial workflows, managing diverse stakeholder expectations, and maintaining data quality throughout the study. They must also handle tight timelines and adapt quickly to regulatory changes or sponsor requirements. Effective communication with both technical teams and clinical staff is crucial to overcoming these obstacles and ensuring successful project delivery.

What are the key skills and qualifications needed to thrive as an EDC Project Manager, and why are they important?

To thrive as an EDC Project Manager, you need expertise in clinical data management, project coordination, and a solid understanding of Electronic Data Capture (EDC) systems, usually supported by a degree in life sciences or related fields. Familiarity with EDC platforms like Medidata Rave or Oracle InForm, along with certifications such as PMP or CDISC, is highly valuable. Strong organizational, problem-solving, and communication skills help you effectively lead cross-functional teams and manage client expectations. These competencies ensure successful EDC project delivery, regulatory compliance, and high-quality clinical trial data.

What are EDC Project Managers?

EDC Project Managers are professionals who oversee the planning, execution, and monitoring of projects related to Electronic Data Capture (EDC) systems, primarily within clinical research and pharmaceutical industries. They coordinate between cross-functional teams, manage timelines, ensure regulatory compliance, and address any issues that arise during the data collection process. Their goal is to ensure that EDC systems are implemented efficiently and effectively, supporting the overall success of clinical trials. EDC Project Managers also act as the main point of contact for sponsors and stakeholders, ensuring that project objectives and quality standards are met.

What is the difference between Edc Project Manager vs Electrical Project Manager?

AspectEdc Project ManagerElectrical Project Manager
CertificationsPMP, OSHA, EDC-specific trainingPMP, OSHA, Electrical licenses
Work EnvironmentEnergy, utility, and infrastructure projectsConstruction, industrial, and commercial electrical projects
Industry UsageCommon in energy distribution and utility sectorsCommon in construction and industrial sectors
Job FocusDistribution systems, substations, and energy deliveryBuilding wiring, electrical systems, and installations

The Edc Project Manager primarily oversees energy distribution and utility infrastructure projects, focusing on energy delivery systems. In contrast, the Electrical Project Manager handles a broader range of electrical construction projects, including commercial and industrial wiring. Both roles require similar certifications but differ in industry focus and project types.

What are popular job titles related to Edc Project Manager jobs in California? For Edc Project Manager jobs in California, the most frequently searched job titles are:
What job categories do people searching Edc Project Manager jobs in California look for? The top searched job categories for Edc Project Manager jobs in California are:
What cities in California are hiring for Edc Project Manager jobs? Cities in California with the most Edc Project Manager job openings:
Edc Project Manager jobs near you

Decision Analytics Associate Consultant - Biometrics

ZS

South San Francisco, CA • On-site

$120K - $137K/yr

Full-time

Posted 17 hours ago

Job description

ZS is a place where passion changes lives. As a management consulting and technology firm focused on improving life and how we live it, we transform ideas into impact by bringing together data, science, technology and human ingenuity to deliver better outcomes for all. Here you'll work side-by-side with a powerful collective of thinkers and experts shaping life-changing solutions for patients, caregivers and consumers, worldwide. ZSers drive impact by bringing a client-first mentality to each and every engagement. We partner collaboratively with our clients to develop custom solutions and technology products that create value and deliver company results across critical areas of their business. Bring your curiosity for learning, bold ideas, courage and passion to drive life-changing impact to ZS.
Insights & Analytics
ZS's Insights & Analytics group partners with clients to design and deliver solutions to help them tackle a broad range of business challenges. Our teams work on multiple projects simultaneously, leveraging deep domain expertise, advanced data analytics, and problem-solving techniques. Our recommendations and solutions are fit-for-purpose and based on rigorous research and analysis.
What You'll Do: Decision Analytics Associate Consultant in the Drug Development Practice Area will...
  • Lead, or co-lead workstreams within larger engagements, managing day-to-day activities, timelines, and deliverables while ensuring project quality
  • Drive clinical data and biometrics transformation initiatives across clinical data management, statistical programming, and biostatistics for pharmaceutical sponsors and CROs
  • Work directly with cross-functional teams supporting ongoing and completed Phase I, II, III, and IV clinical trials, contributing to the collection, management, transformation, analysis, and submission of human clinical trial data throughout the study lifecycle
  • Analyze current-state clinical data flows, systems, and standards (e.g., EDC platforms, non-EDC sources, CDISC SDTM, ADaM) and define future-state architectures and processes
  • Design, specify, or oversee data transformation pipelines that take EDC and non-EDC data from sources systems to submission-ready datasets
  • Shape and deliver AI-focused programs that improve how CDM and SP work is performed (e.g., automation of data review, anomaly detection, edit-check optimization, programming productivity, documentation generation)
  • Partner cross-functionally with clinical operations, data management, biostatistics, statistical programming, and IT teams, serving as a bridge between technical analytics and business needs
  • Collaborate with AI, data science, and technology teams

What You'll Bring
  • Bachelor's or master's degree required in any scientific, analytical, or technical discipline with strong record of academic success
  • 3-5 years of relevant post-collegiate experience in clinical data management, statistical programming, biometrics, or related clinical development functions within a pharmaceutical sponsor, biotechnology company, or CRO. Candidates must have direct hands-on experience supporting Phase I, II, III, or IV human clinical trials and working with the systems, processes, and data generated throughout the clinical trial lifecycle. A PhD may substitute in lieu of work experience
  • Demonstrated ability to lead workstreams, gather and manage requirements, and collaborate with cross-functional and client stakeholders in a structured, project-delivery environment
  • Ability to act as a client-facing consultant, communicating technical concepts to non-technical audiences and supporting project delivery
  • Hands-on experience with clinical trial datasets, including EDC (e.g., Medidata Rave, Veeva EDC) and non-EDC sources (e.g., central laboratory data, ECG, ePRO/eCOA, imaging, PK/PD, wearables, real-world data)
  • Demonstrated experience supporting the execution, management, analysis, or submission of data from Phase I-IV human clinical trials. Strong understanding of GCP, clinical trial operations, and regulatory expectations for analysis and submission datasets
  • Familiarity with clinical trial data standards (e.g., CDISC, SDTM) and biological/RWE datasets used for reuse in clinical analytics
  • Interest in and exposure to AI, automation, or advanced analytics in R&D/CDM/biometrics, and motivation to help clients adopt AI-enabled ways of working from source to submission
  • Fluency in English
  • Client-first mentality
  • Intense work ethic
  • Collaborative spirit and problem-solving approach

Required: Experience directly supporting human clinical trials (Phase I-IV) through clinical data management, statistical programming, biometrics, clinical operations, or related functions. Experience limited to preclinical research, observational studies, real-world evidence, healthcare analytics, or non-interventional data environments will not meet the requirements for this role.
How you'll grow:
  • Cross-functional skills development & custom learning pathways
  • Milestone training programs aligned to career progression opportunities
  • Internal mobility paths that empower growth via s-curves, individual contribution and role expansions

Perks & Benefits:
At ZS, your growth matters. We offer a comprehensive total rewards package that supports your health and well-being, financial future, time away, and professional development. With robust skills-building programs, multiple career progression paths, internal mobility, and a deeply collaborative culture, you'll have the opportunity to do meaningful work, expand your capabilities, and thrive as part of a global community. For details on total rewards in United States, visit ZS US office locations | Where we work | ZS.
Hybrid working model:
We are committed to giving our employees a flexible and connected way of working. A flexible and connected ZS allows us to combine work from home and on-site presence at clients/ZS offices for the majority of our week. The magic of ZS culture and innovation thrives in both planned and spontaneous face-to-face connections.
Travel:
Travel is a requirement at ZS for client facing ZSers; business needs of your project and client are the priority. While some projects may be local, all client-facing ZSers should be prepared to travel as needed. Travel provides opportunities to strengthen client relationships, gain diverse experiences, and enhance professional growth by working in different environments and cultures.
Considering applying?
At ZS, we honor the visible and invisible elements of our identities, personal experiences, and belief systems-the ones that comprise us as individuals, shape who we are, and make us unique. We believe your personal interests, identities, and desire to learn are integral to your success here. We are committed to building a team that reflects a broad variety of backgrounds, perspectives, and experiences. Learn more about our inclusion and belonging efforts and the networks ZS supports to assist our ZSers in cultivating community spaces and obtaining the resources they need to thrive.
If you're eager to grow, contribute, and bring your unique self to our work, we encourage you to apply.
ZS is an equal opportunity employer and is committed to providing equal employment and advancement opportunities without regard to any class protected by applicable law.
To complete your application:
Candidates must possess or be able to obtain work authorization for their intended country of employment. An on-line application, including a full set of transcripts (official or unofficial), is required to be considered.
NO AGENCY CALLS, PLEASE.
Find Out More At:
www.zs.com

About ZS

Sourced by ZipRecruiter

Industry

Business management consulting

Company size

10,000+ Employees

Headquarters location

Evanston, IL, US

Year founded

1983

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