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Ctm Jobs (NOW HIRING)

Vor Bio

Senior/Clinical Trial Manager (CTM)

Boston, MA

$175K - $195K/yr

CTM: Minimum of 5 to 7 years of experience in clinical research with 1-2 years managing trials in the biotech/pharma industry and/or prior CRO experience * Sr. CTM: Minimum of 7+ years of experience ...

Vor Bio

Senior/Clinical Trial Manager (CTM)

Boston, MA · On-site

CTM: Minimum of 5 to 7 years of experience in clinical research with 1-2 years managing trials in the biotech/pharma industry and/or prior CRO experience * Sr. CTM: Minimum of 7+ years of experience ...

Syneos Health

CTM - Future Roles (US)

Morrisville, NC · On-site

CTM - Future Roles (US) Syneos Health ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and ...

Google

Product Manager, CTM Intelligence

Sunnyvale, CA · On-site

The Communications and Time Management (CTM) Intelligence team sits at the heart of the "AI-First" Workspace evolution. We are responsible for building the intelligence layer that understands user ...

IQVIA

CTM Technician

Marietta, GA · On-site

$25K - $53K/mo

Job Overview Assemble laboratory test kits for use by investigators to collect data on clinical trials participants. Work performed is in accordance with ICH E6 Guideline for Good Clinical Practice.

Ruri Software Technologies LLC

SAP APO

Beaverton, OR · On-site

Minimum 5 projects in APO SNP Heuristics and CTM implementations. * Mandatory 3 projects work experience in APO SNP CTM. * Should be a seasoned professional in understanding & implementing CTM ...

Syneoshealth

CTM - Future Roles (US)

Morrisville, NC · On-site

CTM - Future Roles (US) Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and ...

IQVIA, Inc.

CTM Technician

Marietta, GA · On-site

$25K - $53K/mo

Job Overview Assemble laboratory test kits for use by investigators to collect data on clinical trials participants. Work performed is in accordance with ICH E6 Guideline for Good Clinical Practice.

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How much do ctm jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for ctm in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.

What are some common challenges faced by Clinical Trial Managers when overseeing multi-site studies, and how can these be addressed?

Clinical Trial Managers often encounter challenges such as maintaining consistent communication across multiple sites, ensuring protocol adherence, and managing timelines. These challenges can be addressed by establishing clear lines of communication, utilizing centralized project management tools, and holding regular meetings with site coordinators. Developing strong relationships with site staff and proactively identifying potential issues can also help CTMs keep studies on track and maintain data quality.

What is a Clinical Trial Manager?

Clinical Trial Managers (CTMs) are professionals responsible for overseeing and coordinating the planning, implementation, and management of clinical trials. They ensure that trials are conducted according to regulatory guidelines, study protocols, and timelines, while maintaining high standards for patient safety and data integrity. CTMs manage teams, budgets, site selection, and communications between sponsors, investigators, and regulatory bodies throughout the course of a clinical study.

What is the difference between Ctm vs Construction Project Coordinator?

AspectCtmConstruction Project Coordinator
Required CredentialsTypically requires certifications like OSHA, OSHA 30-hour, or specific trade licensesOften requires certifications such as OSHA, PMP, or related project management credentials
Work EnvironmentOn-site construction sites, industrial settings, or manufacturing facilitiesConstruction sites, offices, and project management offices
Employer & Industry UsageUsed mainly in manufacturing, industrial, or construction sectorsCommonly employed in construction firms, engineering companies, and project management firms

The main difference between a Ctm and a Construction Project Coordinator lies in their focus areas. Ctm roles often emphasize technical and safety certifications within industrial or manufacturing environments, while Construction Project Coordinators focus on managing project timelines, budgets, and coordination within construction projects. Both roles require safety knowledge and some project management skills, but their day-to-day responsibilities and industry contexts differ.

What are the key skills and qualifications needed to thrive as a Clinical Trial Manager, and why are they important?

To thrive as a Clinical Trial Manager, you need a strong background in life sciences or a related field, extensive knowledge of clinical trial processes, and experience with regulatory compliance, often supported by a relevant degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications like GCP (Good Clinical Practice) are typically required. Excellent organizational, leadership, and communication skills are vital for effectively managing teams and collaborating with stakeholders. These skills and qualifications ensure the successful planning, execution, and oversight of clinical trials while maintaining regulatory standards and patient safety.
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Ctm jobs near you
Infographic showing various Ctm job openings in the United States as of August 2026, with employment types broken down into 89% Full Time, 7% Part Time, and 4% Contract. Highlights an 84% Physical, 2% Hybrid, and 14% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Senior Clinical Trial Manager (CTM)

Praxis Precision Medicines, Inc.

OR • On-site, Remote

Other

Re-posted 5 hours ago

Job description

Senior Clinical Trial Manager (CTM) 

Location:   This position may be performed remotely with travel to the Boston area as needed.   

Position Summary 

This role will be responsible for project management in the initiation, execution and close out of domestic and international clinical studies, including study concept and design, feasibility assessments, study start-up, contract and budget oversight, data exchange and support of data analysis and interpretation. 

This position requires both the knowledge and experience to work within established clinical trial paradigms while exploring and embracing new approaches to conducting research to support data aggregation and analysis to advance patient care. The Sr. CTM will participate on clinical project teams to achieve quality results in a cost-effective and timely manner. S/he will be a key team member to establish key practices and procedures for the clinical team. 

Primary Responsibilities 

  • Manage study activities in the successful execution of clinical trials from protocol concept to clinical study report, complying with Good Clinical Practice (GCP) guidelines and international regulations 
  • Manage strategic engagement with key collaborators 
  • Set-up and oversee clinical trial-related trackers such as regulatory documents, trial master file (TMF), startup progress, screening/enrollment, study invoices/payments, project budgets, etc. 
  • Key contributor to IRB/EC and regulatory submissions 
  • Oversee TMF reviews to ensure completeness and inspection readiness 
  • Regularly review documents to ensure adherence to Clinical Operations and/or project specific quality requirements (e.g. SOPs, work practices, training guides) 
  • Identify and mitigate against study risks, escalating as necessary 
  • Direct initiatives to identify and implement best practices and continuous improvement plans in clinical development 

Education and Professional Experience 

  • Bachelor's degree in a scientific field required; advanced scientific degree a plus 
  • 5+ years directly managing clinical trials in Sponsor or CRO setting 
  • In-depth knowledge of clinical trial operations, ICH, GCP Guidelines and other applicable regulatory requirements 
  • Experience directing members of clinical operations teams 
  • Experience working in a team across multiple functional areas (e.g., Quality Assurance, Data Management, Biostats, Medical Writing, Safety, Clinical Supply, Finance) 

Other Essentials and Key Success Factors 

  • Intellectual curiosity, innovation and creative problem solving with an entrepreneurial spirit 
  • Ability to think critically in fast-paced projects with a keen sense of urgency and demonstrated ability to problem solve 
  • Self-motivated and able to work autonomously, as well as a member of a collaborative team 
  • Highly-organized and detail-oriented with a passion to deliver quality results 
  • Strong verbal and written communication skills with an ability to build relationships internally and externally 
  • Highest levels of professionalism, confidence, personal values and ethical standards 

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