Understanding of cloud cost management principles and how they apply to observability data and ... Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does ...
New

Understanding of cloud cost management principles and how they apply to observability data and ... Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does ...
New
Understanding of cloud cost management principles and how they apply to observability data and ... Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does ...
New
Lead clinical data management activities for multiple complex studies, from study startup to database lock and final reporting. * Develop and manage data management timelines for multiple projects ...
Lead clinical data management activities for multiple complex studies, from study startup to database lock and final reporting. * Develop and manage data management timelines for multiple projects ...
San Diego, CA · On-site
The Clinical Data Manager will ensure timely conduct of Clinical Data Management activities for assigned studies according to protocols, industry standards and guidelines, Standard Operating ...
New
Quick apply
San Diego, CA · On-site
The Clinical Data Manager will ensure timely conduct of Clinical Data Management activities for assigned studies according to protocols, industry standards and guidelines, Standard Operating ...
New
Lead clinical data management activities for multiple complex studies, from study startup to database lock and final reporting. * Develop and manage data management timelines for multiple projects ...
Lead clinical data management activities for multiple complex studies, from study startup to database lock and final reporting. * Develop and manage data management timelines for multiple projects ...
Lead clinical data management activities for multiple complex studies, from study startup to database lock and final reporting. * Develop and manage data management timelines for multiple projects ...
Lead clinical data management activities for multiple complex studies, from study startup to database lock and final reporting. * Develop and manage data management timelines for multiple projects ...
San Diego, CA · On-site +1
Description The Clinical Data Manager will ensure timely conduct of Clinical Data Management activities for assigned studies according to protocols, industry standards and guidelines, Standard ...
New
San Diego, CA · On-site +1
Description The Clinical Data Manager will ensure timely conduct of Clinical Data Management activities for assigned studies according to protocols, industry standards and guidelines, Standard ...
New
The Clinical Data Manager (CDM) handles project management documentation, clinical data management activities, and system implementations for EDETEK's eClinical, and may be assigned work on other ...
The Clinical Data Manager (CDM) handles project management documentation, clinical data management activities, and system implementations for EDETEK's eClinical, and may be assigned work on other ...
San Francisco, CA · On-site
Clinical Data Manager will be responsible for all aspects of clinical trial data management from study start up through database lock and study close * This includes the EDC build and user acceptance ...
San Francisco, CA · On-site
Clinical Data Manager will be responsible for all aspects of clinical trial data management from study start up through database lock and study close * This includes the EDC build and user acceptance ...
Clinical Data ManagerJob Title Clinical Data Manager Job Summary We are seeking a detail-oriented Clinical Data Manager to oversee the collection, validation, management, and quality of clinical ...
Clinical Data ManagerJob Title Clinical Data Manager Job Summary We are seeking a detail-oriented Clinical Data Manager to oversee the collection, validation, management, and quality of clinical ...
The Clinical Data Manager will plan and oversee all data management activities across assigned studies relatedcompaniondiagnostics (CDx) development to ensuretimely,accurate, and compliant data ...
The Clinical Data Manager will plan and oversee all data management activities across assigned studies relatedcompaniondiagnostics (CDx) development to ensuretimely,accurate, and compliant data ...
1) Lead clinical data manager with 3 -5 years of Sponsor or CRO or Academic experience 2) Project management experience of clinical trials 3) Understanding of clinical data management processes 4) ...
1) Lead clinical data manager with 3 -5 years of Sponsor or CRO or Academic experience 2) Project management experience of clinical trials 3) Understanding of clinical data management processes 4) ...
Burlington, MA · Hybrid
We are seeking a highly skilled and motivated Clinical Data Manager to join our Clinical Data Management team. Reporting to the Associate Director, the Clinical Data Manager, will play a pivotal role ...
Burlington, MA · Hybrid
We are seeking a highly skilled and motivated Clinical Data Manager to join our Clinical Data Management team. Reporting to the Associate Director, the Clinical Data Manager, will play a pivotal role ...
San Diego, CA · On-site
$110K - $120K/yr
The Clinical Data Manager will ensure timely conduct of Clinical Data Management activities for assigned studies according to protocols, industry standards and guidelines, Standard Operating ...
San Diego, CA · On-site
$110K - $120K/yr
The Clinical Data Manager will ensure timely conduct of Clinical Data Management activities for assigned studies according to protocols, industry standards and guidelines, Standard Operating ...
San Francisco, CA · On-site
Clinical Data Manager will be responsible for all aspects of clinical trial data management from study start up through database lock and study close * This includes the EDC build and user acceptance ...
San Francisco, CA · On-site
Clinical Data Manager will be responsible for all aspects of clinical trial data management from study start up through database lock and study close * This includes the EDC build and user acceptance ...
Princeton, NJ · On-site
Lead clinical data management activities for multiple complex studies, from study startup to database lock and final reporting. * Develop and manage data management timelines for multiple projects ...
Princeton, NJ · On-site
Lead clinical data management activities for multiple complex studies, from study startup to database lock and final reporting. * Develop and manage data management timelines for multiple projects ...
Austin, TX · On-site
$125K - $175K/yr
Faeth Therapeutics is seeking an experienced Clinical Data Manager to support clinical data management activities across two active clinical trials. This individual will play a critical role in ...
Austin, TX · On-site
$125K - $175K/yr
Faeth Therapeutics is seeking an experienced Clinical Data Manager to support clinical data management activities across two active clinical trials. This individual will play a critical role in ...
Austin, TX · Remote
$125K - $175K/yr
Faeth Therapeutics is seeking an experienced Clinical Data Manager to support clinical data management activities across two active clinical trials. This individual will play a critical role in ...
Austin, TX · Remote
$125K - $175K/yr
Faeth Therapeutics is seeking an experienced Clinical Data Manager to support clinical data management activities across two active clinical trials. This individual will play a critical role in ...
Burlington, MA · On-site
$145K - $160K/yr
We are seeking a highly skilled and motivated Clinical Data Manager to join our Clinical Data Management team. Reporting to the Associate Director, the Clinical Data Manager, will play a pivotal role ...
Burlington, MA · On-site
$145K - $160K/yr
We are seeking a highly skilled and motivated Clinical Data Manager to join our Clinical Data Management team. Reporting to the Associate Director, the Clinical Data Manager, will play a pivotal role ...
Austin, TX · Remote
$125K - $175K/yr
Faeth Therapeutics is seeking an experienced Clinical Data Manager to support clinical data management activities across two active clinical trials. This individual will play a critical role in ...
Austin, TX · Remote
$125K - $175K/yr
Faeth Therapeutics is seeking an experienced Clinical Data Manager to support clinical data management activities across two active clinical trials. This individual will play a critical role in ...
Columbia, MD · On-site
Clinical Data Manager City: Columbia, MD Country/Region: United States State: Business Area: Clinical Research Department: Clinical Affairs Employment Type: Full-time Req ID: 10220 Job Title:
Columbia, MD · On-site
Clinical Data Manager City: Columbia, MD Country/Region: United States State: Business Area: Clinical Research Department: Clinical Affairs Employment Type: Full-time Req ID: 10220 Job Title:
Do workers at Merck get paid breaks?
Does Merck pay people when they’re sick?
At Merck, are sick days and vacation days separate paid time off?
Is the health insurance from Merck affordable enough for their workers?
Do people get paid time off at Merck?
How far ahead of time do people find out their work schedule?
Do workers at Merck worry about hours?
Do Merck workers get to choose the shifts they work?
How easy is it for Merck workers to change shifts?
How easy is it to get time off at Merck?
Do Merck managers change schedules at the last minute?
Do jobs at Merck spill into time workers aren’t paid for?
How easy is it to take sick days at Merck?
Is working at Merck good if you’re a parent or caregiver?
Do people at Merck feel treated with respect by their managers?
Do people at Merck get to take their breaks without interruption?
Is it stressful to work at Merck?
Do people at Merck enjoy their jobs?
Do people at Merck recommend working with their team?
Do people get enough training when they start at Merck?
Do people get support to advance at Merck?
Do people think Merck’s headquarters understands what’s happening where they work?
Do workers feel well informed about how Merck is doing?

Full-time
This job post has expired today. Applications are no longer accepted.
8.0
Based on 51 frontline employees who took The Breakroom Quiz
42nd of 86 rated pharmaceutical
We are seeking a visionary and influential technical leader to join as a Principal Engineer for Observability. In this role, you will be the chief architect and evangelist for our company-wide observability strategy. Your mission is to define and drive the adoption of a unified, full-stack observability framework that empowers our product teams to build and operate highly reliable, performant, and resilient services.
This is not just a technical role; it is a strategic one. You will work across organizational boundaries, from engineering teams to senior leadership, to champion a culture of operational excellence. You will be responsible for rationalizing our tooling landscape, eliminating redundancy, and designing a cohesive, self-service observability platform that is easy to consume. If you are passionate about turning complex technical concepts into clear business value and leading large-scale change, this is your opportunity to make a lasting impact.
What You'll DoCreate Strategy: Create, document, and champion a unified, long-term observability strategy for the entire company, covering all telemetry types like metrics, traces, logs, profiles and more.
Architect the Future: Design a cohesive, full-stack observability solution using best-in-class tools and practices. Ensure our architecture promotes a product-oriented approach with a strong focus on self-service capabilities.
Drive Standardization and Consolidation: Actively identify and help decommission redundant or overlapping tools, driving the organization towards a standardized, cost-effective, and easy-to-manage observability service.
Join forces with SRE team: Partner with Site Reliability Engineering (SRE) team, promote their principles, such as defining, measuring, and managing Service Level Objectives (SLOs) and error budgets and how critical Observability for them.
Evangelize and Educate: Clearly and persuasively communicate complex observability topics, benefits, and strategic decisions to senior leadership and stakeholders across IT and business domains.
Lead by Influence: Act as the senior technical expert and thought leader in the observability space. Mentor engineers and guide teams in implementing best practices for instrumentation (OpenTelemetry), monitoring, and incident analysis using AIOps.
Stay on the Cutting Edge: Continuously research industry trends, emerging technologies (like eBPF, OpenTelemetry), and best practices to ensure our observability strategy remains modern and effective.
Education-: Bachelor's degree
Extensive Technical Experience: 10+ years in Observability, software engineering, SRE, or platform engineering, with a proven track record of architecting and implementing large-scale technical solutions.
Deep Observability Expertise: Subject matter expert on Observability practices and collection of all types of telemetry. SME for the tools that support them (e.g., Grafana, Prometheus, Dynatrace, BigPanda, xMatters or others).
Strategic Leadership: Demonstrable experience creating and executing a technical strategy across multiple teams or an entire organization.
SRE and SLO Mastery: Deep, practical knowledge of Site Reliability Engineering principles, with hands-on experience defining, implementing, and managing SLOs and error budgets.
OpenTelemetry Proficiency: Strong understanding and practical experience with the OpenTelemetry standard for instrumentation and telemetry collection.
Multi-Cloud Experience: Experience designing solutions that operate across multiple cloud providers (AWS, Azure, GCP).
Exceptional Communication & Influence: World-class ability to explain highly complex technical concepts to senior executives and non-technical audiences. Proven ability to lead by influence and drive consensus in a large organization.
Tool Rationalization: Experience leading projects to consolidate tooling and migrate teams to a centralized platform.
FinOps Knowledge: Understanding of cloud cost management principles and how they apply to observability data and tooling.
eBPF Knowledge: Familiarity with eBPF for advanced, low-level system observability and performance analysis.
Product Mindset: Experience thinking about internal platforms as products, with a focus on user experience, self-service, and clear documentation.
Unmatched Impact: Define the technical direction for a critical capability across the entire company, directly influencing the reliability of all our products.
Strategic Autonomy: Be the ultimate authority and thought leader in the observability domain with the freedom to shape our future.
Executive Visibility: Work directly with senior leadership to connect deep technical initiatives with strategic business outcomes.
Culture: Join a forward-thinking organization that invests in technical excellence and empowers its leaders to drive meaningful change.
Amazon Web Services (AWS), Cloud Infrastructure, Cloud Technology, Cybersecurity, Emerging Technologies, Executive Visibility, FinOps Operating Model, Methods and Tools, Operational Excellence, Platform Engineering, Reliability Engineering, Requirements Management, Software Development, Software Development Life Cycle (SDLC), Solution Architecture, Stakeholder Engagement, Strategic Leadership, Strategic Planning, System Designs, Technical Advice, Telemetry
Preferred Skills:Preferred skills are outlined in the main job description.
San Francisco Residents Only:We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance
Los Angeles Residents Only:We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance
Search Firm Representatives Please Read CarefullyMerck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities.
As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:
EEOC Know Your Rights (https://www.eeoc.gov/sites/default/files/2022-10/22-088_EEOC_KnowYourRights_10_20.pdf)
EEOC GINA Supplement
We are proud to a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.
Learn more about your rights, including under California, Colorado and other US State Acts (https://www.msdprivacy.com/us/en/CCPA-notice/)
Employee Status:Regular
Relocation:No relocation
VISA Sponsorship:No
Travel Requirements:10%
Flexible Work Arrangements:Remote
Shift:1st - Day
Valid Driving License:No
Hazardous Material(s):N/A
Job Posting End Date:07/31/2026
***A job posting is effective until 11:59:59PM on the day** BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Requisition ID:R403622
Sourced by ZipRecruiter
Pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing
10,000+ Employees
Rahway, NJ, US