ZipRecruiter

Log In

1

Merck Clinical Operations Manager Jobs in Oregon

PSI CRO

Clinical Operations Manager

PSI is seeking an experienced and people-focused Clinical Operations Manager to join our team. In this leadership role, you will be responsible for the management, development, and operational ...

PSI CRO

Clinical Operations Manager

OR · On-site +1

PSI is seeking an experienced and people-focused Clinical Operations Manager to join our team. In this leadership role, you will be responsible for the management, development, and operational ...

BetterHelp

OR

As a Clinical Operations Manager at BetterHelp, you'll join a diverse team of licensed clinicians, engineers, product pros, creatives, marketers, and business leaders who share a passion for ...

New

AMSURG

Director, Clinical Operations - Northeast Remote Company Overview: AMSURG is an independent leader ... Manages review and approval of corporate and clinical policies and procedures at the center level.

Amsurg

Director, Clinical Operations - Northeast Remote Company Overview: AMSURG is an independent leader ... Manages review and approval of corporate and clinical policies and procedures at the center level.

Peregrine Team

Clinic Operations Manager

Portland, OR · On-site

This role bridges clinical and administrative functions, ensuring that the team operates ... Manage day-to-day clinic operations including scheduling, staffing, and workflow * Oversee client ...

next page

Showing results 1-20

All JobsMerck Clinical Operations JobsMerck Clinical Operations Manager JobsMerck Clinical Operations Manager Jobs in Oregon

Merck Clinical Operations Manager information

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 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 Clinical Operations Manager at Merck 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 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 Oregon? For Merck Clinical Operations Manager jobs in Oregon, the most frequently searched job titles are:
What job categories do people searching Merck Clinical Operations Manager jobs in Oregon look for? The top searched job categories for Merck Clinical Operations Manager jobs in Oregon are:
What cities in Oregon are hiring for Merck Clinical Operations Manager jobs? Cities in Oregon with the most Merck Clinical Operations Manager job openings:
Merck Clinical Operations Manager jobs near you

Clinical Operations Manager

PSI CRO

On-site, Remote

Full-time

Posted 25 days ago

Job description

Company Description

PSI is a leading Contract Research Organization with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees.  We focus on delivering quality and on-time services across a variety of therapeutic indications.

Job Description

PSI is seeking an experienced and people-focused Clinical Operations Manager to join our team.

In this leadership role, you will be responsible for the management, development, and operational oversight of CRA staff. You will lead and mentor a high-performing team while ensuring efficient resource utilization, operational excellence, and the successful delivery of clinical trials. This position requires a collaborative leader who is passionate about developing people, driving quality, and partnering across functions to support study execution.

This is a home-based role based in the United States. 

The scope of responsibilities will include:

  • Line manage, coach, mentor, and develop Clinical Research Associates across multiple experience levels.
  • Manage hiring, onboarding, performance management, and professional development activities.
  • Oversee resource allocation, workload planning, and utilization across clinical trials.
  • Collaborate with Project Managers and cross-functional teams to ensure successful study delivery.
  • Monitor staff performance and support operational efficiency through established departmental metrics.
  • Implement departmental quality controls and contribute to the development and continuous improvement of quality systems and processes.
  • Prepare for and participate in internal audits, sponsor audits, and regulatory inspections.
  • Support trial execution by resolving operational challenges and facilitating communication between project teams and investigational sites.
  • Participate in feasibility assessments for new and ongoing studies.
  • Support business development activities, including client meetings, networking events, and operational discussions, as needed.
Qualifications
  • MD, PharmD, or a university degree in Life Sciences, or an equivalent combination of education, training, and experience.
  • Minimum of 5 years of clinical research industry experience, including demonstrated team management or people leadership experience.
  • Previous experience working independently as an onsite Clinical Research Associate (CRA) is required.
  • Previous experience managing or mentoring clinical research professionals in a CRO, sponsor, or related clinical research environment.
  • Strong leadership, coaching, and employee development skills.
  • Experience with resource planning, workload management, and performance management.
  • Working knowledge of ICH-GCP, applicable regulatory requirements, and clinical trial operations.
  • Experience supporting audits, inspections, and quality initiatives is preferred.
  • Excellent communication, organizational, and problem-solving skills.
  • Proficiency with Microsoft Office applications and clinical research systems.
  • Advanced English proficiency (written and spoken).
  • Strong interpersonal skills with the ability to build trust, foster collaboration, and develop high-performing teams.
Additional Information

All your information will be kept confidential according to EEO guidelines.

Apply