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Merck Clinical Operations Manager Jobs in New York

Brooklyn Health

Clinical Operations Manager

Manhattan, NY · On-site

$90 - $130/hr

About the role We're hiring a Clinical Operations Manager to oversee eCOA deployments in CNS clinical trials. This position sits within the Operations team. It is an in-person role at our NoHo office.

Conduit Health

Clinical Operations Manager

New York, NY · On-site

$75K - $120K/yr

You partner naturally with Clinical Operations and report clearly to the Ops Manager on provider performance during and after onboarding. * Compliance-Minded: You understand healthcare regulations ...

Zealthy

Clinical Operations Manager

Manhattan, NY · On-site

We are actively looking for a full-time Operations Manager. Please note that this is a full-time, ... Analyze key operational and clinical data to identify areas for improvement and inform decision ...

Zealthy

Clinical Operations Manager

Manhattan, NY · On-site

We are actively looking for a full-time Operations Manager. Please note that this is a full-time, ... Analyze key operational and clinical data to identify areas for improvement and inform decision ...

Zealthy

Clinical Operations Manager

New York, NY · On-site

We are actively looking for a full-time Operations Manager. Please note that this is a full-time, ... Analyze key operational and clinical data to identify areas for improvement and inform decision ...

Verana Health

Operations Manager

New York, NY · Hybrid

Clinicians utilize these insights to improve the quality of care and quality of life for patients ... Merck Global Health Innovation Fund. Join us to bring innovation at scale and improve patient ...

AMC Health

VP, Clinical Operations

New York, NY · On-site

Data & Performance Management * Establish operational metrics and KPIs supporting clinical program performance. * Monitor performance data to identify trends and opportunities for improvement.

Altro Health

Clinical Operations Contractor

New York, NY · On-site +1

$25 - $40/hr

About Us Altro powers the next generation of wellness businesses with clinical infrastructure built for growth. We're building a platform that enables wellness businesses to offer clinical services ...

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Merck Clinical Operations Manager information

What does a Merck clinical operations manager do?

A Merck Clinical Operations Manager oversees the planning, execution, and management of clinical trials to ensure they are conducted efficiently, ethically, and in compliance with regulatory requirements. They coordinate cross-functional teams, manage budgets and timelines, and serve as a key liaison between internal stakeholders and external partners. Their role is critical in ensuring that clinical studies generate reliable data to support the development and approval of new medicines.

How does a Merck clinical operations manager typically collaborate with cross-functional teams during a clinical trial?

As a Clinical Operations Manager at Merck, you will regularly collaborate with cross-functional teams such as clinical research associates, data management, regulatory affairs, medical writing, and biostatistics. Your role involves facilitating clear communication to ensure trial milestones are met, addressing operational challenges, and aligning on project goals. You will often lead meetings, coordinate with internal and external stakeholders, and ensure that all teams are updated on timelines, compliance, and protocol changes. This collaborative environment is essential for delivering high-quality clinical studies efficiently and in accordance with regulatory standards.

What are the key skills and qualifications needed to thrive as a Merck clinical operations manager, and why are they important?

To thrive as a Merck Clinical Operations Manager, you need a strong background in clinical research, project management, and a relevant degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), regulatory compliance, and certifications like PMP or GCP are commonly required. Exceptional leadership, problem-solving, and communication skills distinguish top performers in this role. These skills ensure the effective execution of clinical trials, regulatory adherence, and successful cross-functional team collaboration.

What is the difference between Merck Clinical Operations Manager vs Merck Clinical Research Associate?

AspectMerck Clinical Operations ManagerMerck Clinical Research Associate
ResponsibilitiesOversees clinical trial operations, manages teams, ensures compliance, and coordinates with stakeholders.Supports site activities, monitors trial progress, and ensures data accuracy at clinical sites.
Required CredentialsBachelor's degree in life sciences, project management experience, knowledge of GCP guidelines.Bachelor's degree in health sciences or related field, clinical trial monitoring experience.
Work EnvironmentOffice-based with site visits, team management, strategic planning.Primarily site visits, monitoring activities, and data collection.

The Merck Clinical Operations Manager focuses on overseeing entire clinical trial processes and managing teams, while the Merck Clinical Research Associate primarily supports site-level activities and monitors trial progress. Both roles require relevant clinical experience and knowledge of GCP guidelines, but differ in scope and responsibilities.

What are popular job titles related to Merck Clinical Operations Manager jobs in New York?

For Merck Clinical Operations Manager jobs in New York, the most frequently searched job titles are:

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The top searched job categories for Merck Clinical Operations Manager jobs in New York are:

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Cities in New York with the most Merck Clinical Operations Manager job openings:

Merck Clinical Operations Manager jobs near you

Clinical Operations Manager

Manhattan, NY • On-site

Brooklyn Health
See more jobs at Brooklyn Healthexternal

$90 - $130/hr

Other

Posted 9 days ago

Job description

About Brooklyn Health

Brooklyn Health is solving the measurement problem in mental health through accurate, objective, and sensitive measurement of symptoms, enabling precision neuroscience in clinical research and patient care. The company’s Willis platform is modernizing the technology stack for CNS clinical trials, improving endpoint quality and reducing placebo response. Brooklyn Health is backed by leading healthcare and technology investors including HealthX Ventures, Metrodora Ventures, Story Ventures, RiverPark Ventures, Laconia Capital, Everywhere Ventures and others. For more information, visit www.brooklyn.health.

About the role

We’re hiring a Clinical Operations Manager to oversee eCOA deployments in CNS clinical trials. This position sits within the Operations team. It is an in-person role at our NoHo office.

Responsibilities
  • Oversee end-to-end management and delivery of eCOA and additional Brooklyn Health solutions, including rater certification, scale licensing, and data monitoring.
  • Coordinate with customers on timelines, project specifications, testing, and go-live readiness.
  • Perform clinical protocol review to ensure appropriate software and service delivery across solutions.
  • Maintain tracking and reporting on project deliverables, manage issue resolution, and support ongoing project updates as needed.
  • Collaborate with internal Science, Product, and Engineering teams to ensure successful project delivery.
  • Drive process improvement and project management best practices.
Requirements
  • Critical thinking skills to navigate complex issues; experience with cross-functional work
  • The ability to gain support from other teams and ensure alignment to business initiatives, processes, and issue resolution
  • Project planning and budget management to effectively manage individual studies
  • Proclivity for meticulous documentation and proficiency with project management tools like Asana
  • A genuine interest in addressing the mental healthcare crisis in the United States
  • Ability to be in-office full-time in New York City
  • 2+ years project management experience in clinical research, eCOA/ePRO, clinical technologies, or CRO setting
Nice-to-haves
  • Prior experience as a site study coordinator
  • Strong understanding of clinical study lifecycle, data flow, and regulatory compliance requirements
  • Excellent organizational, communication, and cross-functional coordination skills
  • Ability to work independently and operate effectively in a fast-paced, remote environment
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