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Gcp Program Manager Jobs (NOW HIRING)

NLB Services

Program Manager

Atlanta, GA · On-site

... upgrade programs Cyber Incident Response Manage projects that enhance incident response ... AWS, Azure, GCP) Knowledge of PKI, certificate lifecycle management, and identity security ...

Koantek

Technical Program Manager

Chandler, AZ · On-site

$127K - $164K/yr

Technical Program Manager (TPM) About Us We're on a mission to turn ambitious ideas into impactful ... Strong understanding of software development life cycles, cloud platforms (AWS, Azure, or GCP ...

Game Plan Tech

Program Manager

Washington, DC · On-site +1

Program Manager Location: Washington, DC Metro Area Role Overview Game Plan Tech is seeking an ... Experience managing projects related to Cloud Landing Zones (e.g., AWS, Azure, GCP), cloud-native ...

Game Plan Tech

Program Manager

Washington, DC · On-site

Program Manager Location: Washington, DC Metro Area Role Overview Game Plan Tech is seeking an ... Experience managing projects related to Cloud Landing Zones (e.g., AWS, Azure, GCP), cloud-native ...

Koantek LLC

Technical Program Manager

Chandler, AZ · On-site

$131K - $170K/yr

The Impact You'll Make As our Technical Program Manager, you'll be the bridge between vision and ... Strong understanding of software development life cycles, cloud platforms (AWS, Azure, or GCP ...

Uber Technologies, Inc.

Program Manager

New York, NY · On-site

... GCP) for deploying and managing machine learning models, orchestrating data workflows, and scaling compute resources efficiently; * Qualitative analysis of text data, including thematic analysis and ...

Uber Technologies, Inc.

Program Manager

New York, NY · On-site +1

... GCP) for deploying and managing machine learning models, orchestrating data workflows, and scaling compute resources efficiently; * Qualitative analysis of text data, including thematic analysis and ...

Fivetran

Technical Program Manager, Security

Oakland, CA · On-site

$148K - $191K/yr

Fivetran is a multi-cloud environment operating on AWS, GCP, and Azure. You will help select ... Running the Dependency management and image hardening programs * Using AI to contribute to the ...

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Gcp Program Manager information

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$38.5K

$107.5K

$157K

How much do gcp program manager jobs pay per year?

As of Sep 11, 2026, the average yearly pay for gcp program manager in the United States is $107,460.00, according to ZipRecruiter salary data. Most workers in this role earn between $79,500.00 and $132,500.00 per year, depending on experience, location, and employer.

What are popular job titles related to Gcp Program Manager jobs?

For Gcp Program Manager jobs, the most frequently searched job titles are:

Infographic showing various Gcp Program Manager job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 17% Part Time, and 3% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $107,460 per year, or $51.7 per hour.

Clinical Program Manager

Redwood City, CA • Hybrid

Revolution Medicines
See more jobs at Revolution Medicinesexternal

Full-time

Re-posted 3 days ago

Job description

The Opportunity:

This is a unique opportunity for a Clinical Operations Professional. As a Clinical Program Manager (CPM), you will be responsible for acting as a central contact for the Clinical Study Team(s) and assist with the execution and management of Revolution Medicines (RevMed) clinical trials.

  • Adhere to Clinical Standard Operating Procedures (SOP), Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) Guidelines.

  • Be a team leader, providing guidance and oversight for the successful management of all aspects of clinical trials within timelines and designated program budgets.

  • Partner with cross-functional teams to manage, adjust, and revise project timelines and budgets as needed.

  • Analyze data health metrics to be shared with stakeholders.

  • Actively partner with cross-functional teams and vendors to drive the query resolution and data listings review process to meet objectives in a timely and efficient process.

  • Conduct risk management, contingency, and scenario planning.

  • Supervise, communicate project status/issues, and problem solve to ensure project team goals are met.

  • Participate in the development of all study-related documentation, including study protocols.

  • Actively contributes in the selection and management of contract research organizations (CROs) and/or vendors, including development of requests for proposals (RFPs).

  • Use all available tools to track, oversee, and communicate on program status to all key stakeholders.

  • Participate in other Clinical Operations activities as appropriate.

  • Leads a larger, more complex trial with some oversight from senior members of Clinical Operations.

  • With minimal support, lead cross-functional Clinical Study Execution Team (CSETs).

  • Participate in and contribute to SOP development, implementation, and training.

  • Support junior team members through mentorship.

Required Skills, Experience and Education:

  • RN or Bachelor's or Masters degree in biological sciences or health-related field required.

  • 8+ years direct Clinical Operations experience in the pharmaceutical or biotech industry, preferably in Clinical Operations or Clinical Research-related experience. Relevant indirect experiences may also meet the requirement.

  • Minimum of 4 years of cross-functional study management or related leadership experience in life sciences, including multiple years' experience managing project teams.

  • Strong working knowledge of FDA Regulations, ICH Guidelines, and GCP.

  • Proven ability to successfully start-up, manage, and close-out clinical trials, including authoring clinical study and regulatory documentation and SOPs.

  • Experience in selection of CROs/vendors and management of external resources.

  • Thrives in a collaborative team setting that demonstrates flexibility required to maintain a fast pace and is driven by a desire to deploy innovative approaches and technologies in a high-energy environment.

  • Be solution-oriented by anticipating obstacles and difficulties, and proactively providing risk assessment and mitigation strategies to achieve project goals.

  • Excellent written/verbal communication and interpersonal skills.

  • High sense of priority and commitment to excellence in the successful execution of deliverables.

  • Ability to analyze operational data, contribute with a mind on quality, timeliness and fiscal responsibility, make and drive decisions, multi-task, prioritize tasks, anticipate challenges, and execute on goals as a member of an interdisciplinary team.

  • Demonstrate proficiency in Microsoft Office Suite (Outlook, MS Word, Excel, PowerPoint); MS Project and/or Smartsheet a plus.

  • Travel may be required (~25%).

Preferred Skills:

  • Familiarity working with vendor systems/portals (e.g., eTMF, EDC, IRT, CTMS).

  • Oncology experience, early and/or late stage, strongly preferred.

  • Knowledge and/or familiarity with Ex-US region(s) clinical trial operations.

  • Some experience mentoring jr staff. 

    #LI-Hybrid  #LI-DN1

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