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Contract Ctm Clinical Trial Manager Jobs (NOW HIRING)

Impulse Dynamics

Clinical Trial Manager

Marlton, NJ

$95K - $115K/yr

For CTM: Minimum of 4 years of progressive experience in clinical operations, clinical trial management, or project management within the pharmaceutical, biotechnology, medical device, or contract ...

Vor Bio

Senior/Clinical Trial Manager (CTM)

Boston, MA

$175K - $195K/yr

Vor Biopharma is seeking a Clinical Trial Manager/Sr. Clinical Trial Manager who will be ... Participate in the selection, training, and evaluation of study personnel (contract and internal ...

Allen Spolden

Clinical Trial Manager

Philadelphia, PA · On-site

Clinical Trial Manager The role: The Clinical Trial Manager is responsible for the delivery of all ... The CTM oversees the clinical portion of the budget, develops monitoring plans & tools, trains CRAs ...

New

Allen Spolden

Clinical Trial Manager

Philadelphia, PA · On-site

Clinical Trial Manager The role: The Clinical Trial Manager is responsible for the delivery of all ... The CTM oversees the clinical portion of the budget, develops monitoring plans & tools, trains CRAs ...

New

Clinovo

Clinical Trial Manager

Cambridge, MA · On-site

$175K/yr

The Clinical Trial Manager (CTM) plays a key role in the successful execution of clinical research ... CRO & Vendor Management * Act as the primary operational liaison for contract research ...

Kardigan

Clinical Trial Manager

Princeton, NJ · Remote

As a Clinical Trial Manager (CTM), you will be part of the Clinical Operations team reporting to ... Manages CRO and vendor budgets and invoicing procedures according to study contract * Summarizes ...

Prometrika

Clinical Trial Manager

Cambridge, MA · On-site

Responsibilities The Clinical Trial Manager (CTM) works closely with various sponsors, internal ... Manage the feasibility, selection, training and evaluation of study personnel (contract and ...

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Contract Ctm Clinical Trial Manager information

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How much do contract ctm clinical trial manager jobs pay per hour?

As of Aug 31, 2026, the average hourly pay for contract ctm clinical trial manager 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 does a contract clinical trial manager do?

A Contract Clinical Trial Manager (CTM) oversees the planning, execution, and management of clinical trials on a contract basis, typically for pharmaceutical, biotechnology, or clinical research organizations. They ensure trials are conducted according to regulatory guidelines, study protocols, and timelines. CTMs coordinate with study teams, manage budgets, oversee site selection and monitoring, and address any issues that arise during the trial. As contractors, they may work on multiple projects or for different clients, providing flexibility and specialized expertise.

What are the typical challenges faced by contract clinical trial managers when working across multiple clinical studies for different sponsors?

Contract CTMs often manage several clinical trials simultaneously, each with its own sponsor requirements, timelines, and protocols. This can lead to challenges such as balancing competing priorities, adapting to diverse sponsor expectations, and ensuring compliance with varying regulatory standards. Effective time management, strong communication skills, and the ability to quickly familiarize oneself with new therapeutic areas or processes are essential for success. Collaborating closely with cross-functional teams, such as data management, regulatory affairs, and site monitors, is also crucial to keep studies on track and maintain high-quality results.

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

To thrive as a Contract Clinical Trial Manager (CTM), you need a solid background in clinical research, regulatory compliance, project management, and typically a science degree or equivalent experience. Familiarity with clinical trial management systems (CTMS), ICH-GCP guidelines, and often certifications like ACRP or SOCRA are important. Strong leadership, problem-solving, and communication skills help manage teams and collaborate with stakeholders effectively. These skills ensure trials are conducted efficiently, compliantly, and to the highest standards, ultimately supporting successful study outcomes.

What is the difference between Contract Ctm Clinical Trial Manager vs Clinical Research Associate?

AspectContract Ctm Clinical Trial ManagerClinical Research Associate
CredentialsTypically requires a Bachelor's degree in life sciences, with some roles preferring a Clinical Research CertificationRequires a Bachelor's degree in life sciences or related field; certifications like CRA certification are common
Work EnvironmentManages clinical trial sites, oversees trial progress, and liaises with sponsors and vendorsMonitors clinical sites, ensures protocol compliance, and collects data
Employer & Industry UsageUsed by pharmaceutical companies, CROs, and biotech firms for trial management rolesCommonly employed by CROs and pharmaceutical companies for site monitoring roles

The Contract Ctm Clinical Trial Manager focuses on overseeing entire clinical trials, managing teams, and ensuring trial milestones are met. In contrast, the Clinical Research Associate primarily monitors clinical sites and ensures compliance. Both roles require similar educational backgrounds and certifications but differ in scope and responsibilities.

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Contract Ctm Clinical Trial Manager jobs near you
Infographic showing various Contract Ctm Clinical Trial Manager job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Clinical Trial Manager (contract)

South San Francisco, CA • On-site

ALX Oncology Inc.
Biotechnology Research and Development • 11 - 50 employees
Learn more about ALX Oncology Inc.external

$70/hr

Contractor

Posted 13 days ago

Job description

Reporting to the Executive Director, Clinical Operations, the contract Clinical Trial Manager (CTM) will manage the day-to-day operational execution of global clinical trials from study start-up through closeout. The contract CTM will be responsible for coordinating study activities, managing timelines and vendors, monitoring study and site performance, and working across functions to ensure study milestones and deliverables are achieved on time and to a high standard of quality.
This is a 6- to 12-month contract assignment offering approximately 40 hours per week. The anticipated pay rate is approximately $70 per hour for candidates in the San Francisco Bay Area. Candidates who can work onsite in South San Francisco on Mondays and Tuesdays as part of the company's hybrid work model will be given preference. ADC clinical trial experience strongly preferred.
Qualified contractors should have experience that includes:
  • Managing day-to-day global clinical trial activities from study start-up through conduct and closeout, including timelines, milestones, enrollment, and study performance.
  • Supporting protocol review, feasibility assessments, site selection and activation, and protocol amendment activities.
  • Managing CROs, sites, and clinical vendors, including oversight of plans, deliverables, timelines, budgets, and quality.
  • Overseeing monitoring activities, including monitoring report review, U.S. co-monitoring, site performance, protocol deviations, data queries, and follow-up of significant issues.
  • Identifying operational risks and working cross-functionally to develop and implement mitigation strategies.
  • Leading study team meetings and communicating study progress, risks, decisions, and action items to internal and external stakeholders.
  • Ensuring study conduct and TMF quality are consistent with study protocols, ICH/GCP, applicable regulatory requirements, and inspection-readiness expectations.
  • Clinical operations experience in biotechnology, pharmaceutical, or CRO environments; ADC clinical trial experience strongly preferred.
  • Strong project management, communication, problem-solving, and organizational skills; proficiency with EDC, IRT, CTMS, and eTMF.
  • Ability to work effectively in a small, fast-paced biotech environment.

About ALX Oncology
ALX Oncology (Nasdaq: ALXO) is a clinical-stage biotechnology company advancing a pipeline of novel therapies designed to treat cancer and extend patients' lives. ALX Oncology's lead therapeutic candidate, evorpacept, has demonstrated potential to serve as a cornerstone therapy upon which the future of immuno-oncology can be built. Evorpacept is currently being evaluated across multiple ongoing clinical trials in a wide range of cancer indications. ALX Oncology's second pipeline candidate, ALX2004, is a novel EGFR-targeted antibody-drug conjugate with a differentiated mechanism of action. A Phase 1, dose-escalation trial of ALX2004 is ongoing in patients with EGFR-expressing solid tumors. More information is available at www.alxoncology.com and on LinkedIn @ALX Oncology.

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