ZipRecruiter

Log In

1

Edc Project Manager Jobs in Novato, CA (NOW HIRING)

IQVIA

Senior Data Team Lead (Remote)

San Francisco, CA · Remote

$86K - $217K/yr

... Project Manager . * Proven success managing large global studies (1000+ patients). * Expertise with Medidata Rave, Oracle InForm, or similar EDC systems. * Strong understanding of GCP, ICH, and ...

IQVIA

Senior Data Team Lead (Remote)

Oakland, CA · Remote

$86K - $217K/yr

... Project Manager . * Proven success managing large global studies (1000+ patients). * Expertise with Medidata Rave, Oracle InForm, or similar EDC systems. * Strong understanding of GCP, ICH, and ...

Exelixis

Senior AI Data Scientist I

Alameda, CA

Execute data cleaning, transformation, and standardization tasks across clinical datasets from EDC ... Management, and Clinical Operations to deliver AI/ML project milestones and address study-level ...

Exelixis Inc

Senior AI Data Scientist I

Alameda, CA · On-site

$143.50 - $203/hr

Execute data cleaning, transformation, and standardization tasks across clinical datasets from EDC ... Data Management, and Clinical Operations to deliver AI/ML project milestones and address ...

previous pagenext page

Showing results 21-40

All JobsEdc Project JobsEdc Project Manager JobsEdc Project Manager Jobs in Novato, CA

Edc Project Manager information

See Novato, CA salary details

$45.2K

$120.6K

$190.2K

How much do edc project manager jobs pay per year?

As of Aug 11, 2026, the average yearly pay for edc project manager in Novato, CA is $120,555.00, according to ZipRecruiter salary data. Most workers in this role earn between $92,200.00 and $144,400.00 per year, depending on experience, location, and employer.

Does Edc Project Manager offer remote work options?

The Edc Project Manager role may offer remote work options depending on the employer's policies. Many project management positions can be performed remotely, especially with skills in collaboration tools and virtual communication. Candidates should verify specific job postings for remote work availability.

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 is an EDC project manager?

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 job categories do people searching Edc Project Manager jobs in Novato, CA look for? The top searched job categories for Edc Project Manager jobs in Novato, CA are:
What cities near Novato, CA are hiring for Edc Project Manager jobs? Cities near Novato, CA with the most Edc Project Manager job openings:
Edc Project Manager jobs near you

Sr. Clinical Trial Manager (NS)

Structure Therapeutics

South San Francisco, CA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

This job post has expired today. Applications are no longer accepted.

Job description

About Us:
Structure Therapeutics develops life-changing medicines for patients using advanced structure-based and computational drug discovery technology. The company's platform combines the latest advancements in visualization of molecular interactions, computational chemistry, and data integration to design orally available, superior small molecule medicines that overcome current limitations of biologic and peptide drugs. We are advancing a clinical-stage pipeline of differentiated treatments focused on chronic diseases with high unmet need, including cardiovascular, metabolic, and pulmonary conditions.
Structure Therapeutics is led by an experienced group of international drug innovators and financed by top-tier global life sciences investors. The company completed an initial public offering (IPO) in February 2023. With offices in California and Shanghai, Structure Therapeutics has the benefit of being at the center of life science innovation in both the US and China and capitalizing on the strengths of each geographic location.
Position Summary:
Structure Therapeutics is seeking a highly motivated Sr. Clinical Trial Manager (SCTM) to be part of our Clinical Operations team. This is a unique opportunity to join a growing company committed to converting biologics and peptides into life-changing small molecule medicines for everyone. The SCTM will be responsible for the day-to-day oversight of global clinical trials and will manage internal stakeholders, CROs, multiple service providers, clinical monitors, and clinical trial sites. The SCTM will focus on the management and support of multinational, multicenter, late stage studies and may assume responsibility for additional studies/indications as applicable. The SCTM works closely with and supports the Clinical Development Operations team, receives assignments in the form of objectives, and will ensure deliverables are completed on time and within budget.
This position will also work closely with a cross-functional team based in the US and Shanghai to ensure that clinical trials are conducted in a timely fashion and compliant with SOPs, ICH/GCP, Country specific regulatory guidelines, company goals, and budgets. The SCTM will be responsible for managing various project goals and supporting delivery of a quality clinical trial to meet current business needs and trends.
Job Responsibilities
  • Leads and coordinates global cross-functional study teams through all study stages (start-up, conduct, close-out).
  • In collaboration with internal stakeholders, responsible for helping to drive the RFP and RFI process, analyze service providers, budgets and proposals, conduct bid defense meetings, award services, negotiate and execute complex agreements (i.e., CRO, study related collaboration agreements).
  • Provides oversight and direction to the CRO and service providers to accurately coordinate clinical study activities.
  • Assists with Inspection Readiness activities which may require the development, modification and/or implementation of policies as needed to ensure high quality and integrity in all study activities.
  • Coordinate clinical study timelines with Project management and escalate issues that may impact timelines/ deliverables.
  • Leads and/or participates in the development and review of study documents including, but not limited to, CRF design, project plans, Service Provider Oversight plans, TMF plan.
  • Follows processes and procedures and recommend changes to SOP's and policies to ensure comprehensive and compliant processes in the clinical operations organization.
  • Identifies potential study issues/risks, escalates as needed and recommends/implements
  • Manages study sites and study related activities including but not limited to site feasibility, selection, start up, subject recruitment, enrollment, study management, monitoring report review, site management, trial master files, and data review/clean up.
  • Coordinate with Lead and Finance to track the financial status against budget.
  • Provide regular updates to Study Lead and other stakeholders; Proactively identify, manage, or escalate issues appropriately.
  • Prepares or reviews clinical sections of regulatory submission documents, responses to EC and/or Health Authority questions.
  • Monitors study progress for possible changes in study scope to ensure timely change order implementation and finalization; implementation of PI Training, site monitor training, etc.
  • May have some responsibility for the oversight and management of the study budget including site and service provider budgets.
  • Supervises ongoing communication of operational issues and provides accurate progress reports on assigned activities to Study Management Team and Clinical Development Team.
  • Ensures oversight of data and information in study specific systems EDC, CTMS, eTMF is current and accurate.
  • May lead a cooperative effort on a project team or contribute as a subject matter expert on key projects and initiatives to identify and implement process improvements and standards.
  • Other supportive duties as assigned to achieve operational

Qualifications:
Education
  • Bachelor's degree or equivalent (scientific or healthcare discipline preferred)

Experience
  • Minimum of 7+ years of related industry experience as a Clinical Research Associate or related function with increasing responsibility and scope
  • Minimum of 3+ years study management experience in clinical and drug development
  • Experience in selecting, managing, and overseeing sites, CROs, specialty labs and other service providers in global, multinational studies or programs.
  • Experience in supporting SOP development and implementation is
  • Experience working on global teams is desired, Asia-Pacific and EU highly

Core Competencies, Knowledge and Skill Requirements
  • PC literacy required; MSOffice skills (Outlook, Word, Excel, PowerPoint)
  • In-depth understanding of FDA and EU regulations, ICH Guidelines and GCP requirements governing the conduct of clinical trials.

Travel Required: Up to 30%
Structure Therapeutics Inc. is an Equal-Opportunity Employer.
Structure Therapeutics is committed to fair and equitable compensation practices, and we strive to provide employees with total compensation packages that are market competitive. For this role, the anticipated base pay range is $171,000 - $218,000. The exact base pay offered for this role will depend on various factors, including but not limited to the candidate's geography, qualifications, skills, and experience.
At Structure, base pay is only one part of your total compensation package. The successful candidate will be eligible for an annual performance incentive bonus, new hire equity, and ongoing performance-based equity. Structure Therapeutics also offers various benefits offerings, including, but not limited to, medical, dental, and vision insurance, 401k match, unlimited PTO, and a number of paid holidays including winter shutdown.

Apply