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Merck Clinical Operations Manager Jobs in Austin, TX

AMC Health

VP, Clinical Operations

Austin, TX · On-site

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

Senseye

Director of Clinical Operations

Austin, TX · On-site

$18K - $205K/yr

Manage and coordinate external partners, including CROs, sites, and investigators * Design study ... Experience building or scaling clinical operations functions Benefits * The freedom and trust to ...

Senseye

Director of Clinical Operations

Austin, TX

$18K - $205K/yr

Manage and coordinate external partners, including CROs, sites, and investigators * Design study ... Experience building or scaling clinical operations functions Benefits * The freedom and trust to ...

Senseye, Inc.

Director of Clinical Operations

Austin, TX · On-site

$180 - $205/hr

Manage and coordinate external partners, including CROs, sites, and investigators * Design study ... Experience building or scaling clinical operations functions Benefits * The freedom and trust to ...

Senseye

Director of Clinical Operations

Austin, TX · On-site

$18K - $205K/yr

Manage and coordinate external partners, including CROs, sites, and investigators * Design study ... Experience building or scaling clinical operations functions Benefits * The freedom and trust to ...

DiaSorin

Clinical Operations Coordinator

Austin, TX

Comply with the company's Quality Management System policies and procedures. Perform administrative role for CTMS and related activities. Coordinate clinical operations projects as needed. Track and ...

DiaSorin

Clinical Operations Coordinator

Austin, TX · On-site

... Management System policies and procedures. • Perform administrative role for CTMS and related activities. • Coordinate clinical operations projects as needed. • Track and update site inventory ...

Training Wheels ABA

Operations Manager

Austin, TX · On-site

$70K - $80K/yr

Operations Manager Training Wheels ABA Central Austin & Surrounding Areas, TX Full-Time | Exempt ... Partner with clinical leadership to support parent and family engagement * Monitor and support ...

PDS Health

Operations Manager

Austin, TX · On-site

$24/hr

The role of the Operations Manager Trainee (OMT) is to gain an understanding of the skills and ... staff and clinicians; understands local market drivers and competition * Influencer (active ...

PDS Health

Operations Manager

Austin, TX · On-site

$24/hr

The role of the Operations Manager Trainee (OMT) is to gain an understanding of the skills and ... staff and clinicians; understands local market drivers and competition * Influencer (active ...

PDS Health

Operations Manager

Austin, TX · On-site

$24/hr

The role of the Operations Manager Trainee (OMT) is to gain an understanding of the skills and ... staff and clinicians; understands local market drivers and competition * Influencer (active ...

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All JobsMerck Clinical Operations JobsMerck Clinical Operations Manager JobsMerck Clinical Operations Manager Jobs in Austin, TX

Merck Clinical Operations Manager information

See Austin, TX salary details

$34.7K

$97.2K

$184.9K

How much do merck clinical operations manager jobs pay per year?

As of Aug 25, 2026, the average yearly pay for merck clinical operations manager in Austin, TX is $97,177.00, according to ZipRecruiter salary data. Most workers in this role earn between $71,900.00 and $112,500.00 per year, depending on experience, location, and employer.

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 Austin, TX?

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

What job categories do people searching Merck Clinical Operations Manager jobs in Austin, TX look for?

The top searched job categories for Merck Clinical Operations Manager jobs in Austin, TX are:

What cities near Austin, TX are hiring for Merck Clinical Operations Manager jobs?

Cities near Austin, TX with the most Merck Clinical Operations Manager job openings:

Merck Clinical Operations Manager jobs near you

Clinical Operations Manager

Pinnacle Clinical Research

Austin, TX • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 12 days ago

Job description

Summary: The Clinical Operations Manager is responsible for operational implementation of assigned studies at their research site. The incumbent supervises clinical trial staff and works closely with the Principal Investigator, Site Director and Regional Director, and cross-functional teams to ensure successful completion of research activities. This role serves as the primary liaison between the research site, sponsors, CROs, and other stakeholders while maintaining compliance with regulations.
Duties and Responsibilities:
Clinical Trial Management
  • Oversee daily operations of clinical research staff and studies
  • Coordinate multiple projects with competing priorities and deadlines
  • Monitor adherence to protocols and study timelines
  • Act as primary liaison with sponsors, CROs, and vendors
  • Prepare for and facilitate study monitor visits
Regulatory Compliance
  • Ensure adherence to Standard Operating Procedures (SOPs), FDA regulations, and other regulatory references
  • Maintain subject and document confidentiality and privacy
  • Assist with regulatory submissions and file maintenance
  • Create and implement corrective and preventive action plans when appropriate
Study Documentation
  • Supervise creation and completion of study-related documents
  • Supervise completion of case report forms
  • Supervise documentation of adverse events and subject history
  • Prepare reports as requested
Study Participant Coordination
  • Supervise study assessments with study participants including informed consent
  • Supervise subject screening and recruitment
  • Supervise appointment scheduling and visit implementation
  • Supervise collection of vital signs and study participant assessments
  • Supervise phlebotomy, specimen processing, and biological sample shipping
Resource Management
  • Identify departmental needs for supplies, staffing, and equipment
  • Improve research processes within established guidelines
Supervisory Responsibilities: Directly supervises Clinical Research Coordinators and Research Assistants, ensuring compliance with SOPs and regulations. Carries out supervisory responsibilities according to organizational policies and applicable laws, including:
  • Training employees
  • Planning, assigning, and directing work (with management guidance)
  • Appraising performance
  • Addressing complaints and resolving problems
Education/Experience:
  • High school diploma or GED required; Bachelor's degree preferred
  • Three to five years of experience in a Clinical Research Coordinator role
  • Previous experience managing clinical research coordinators preferred
  • For CNS sites, experience conducting rating scales such as MMSE
Certificates and Licenses:
  • Good Clinical Practice training certification
  • IATA training certification
  • Valid driver's license and insurance
Knowledge, Skills, and Other Abilities:
  • Strong oral and written communication abilities
  • Excellent organizational skills and attention to detail
  • Professional interpersonal skills with a positive demeanor
  • Adaptability to changing priorities
  • Medical knowledge including terminology
  • Thorough understanding of regulations, regulatory guidance, and SOPs
  • Proficiency with Microsoft Office, web browsers, and electronic case report form systems
Work Environment and Physical demands:
The work environment and physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
  • Office/laboratory and clinical environment.
  • Exposure to biological fluids and/or bloodborne pathogens.
  • Personal protective equipment required
  • Occasional domestic and international travel
  • Ability to maintain upright/stationary position for 6-10 hours daily
  • Frequent mobility required.
  • Occasional squatting, kneeling, or bending.
  • Light to moderate lifting (20-50 lbs)
Perks of working at Summit Clinical Research Solutions:
  • 401k
  • Medical, dental, vision, long term disability, short term disability, FSA, and life insurance
  • 3 weeks of paid time off
  • 14 paid company holidays
  • Scrub voucher (for eligible positions)
  • And more!
Summit Clinical Research Solutions is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, disability, gender, national origin, age, genetic information, military or veteran status, sexual orientation, gender identity, marital status or any other protected Federal, State/Province or Local status unrelated to the performance of the work involved.