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Medical Monitor Clinical Trial Jobs (NOW HIRING)

Verastem

Clinical Trial Manager

Boston, MA · On-site

$100K - $125K/yr

Liaise with medical monitor and cross functional team members as necessary and in accordance with ... Global Phase 3 clinical trial management experience * Minimum of 3 years of clinical trial ...

Kymera Therapeutics

Clinical Trial Manager

Watertown, MA · On-site

$115K - $200K/yr

Responsible for management of vendors to support clinical trial execution * Plan, execute, and lead ... Work closely with CRO and Medical Monitor to ensure safety and efficacy data appropriately ...

US Tech Solutions

Medical Monitor IV

Princeton, NJ · On-site

$18.75 - $24/hr

Medical Monitor The Medical Monitor role involves providing clinical development support across ... Review and interpret clinical trial data, including tables, listings, and figures * Support data ...

Verastem Oncology

Clinical Trial Manager

Boston, MA · On-site

$100 - $125/hr

Liaise with medical monitor and cross functional team members as necessary and in accordance with ... Minimum of 3 years of clinical trial experience, including prior experience in oncology clinical ...

New

Verastem

Clinical Trial Manager

Boston, MA · On-site

$100K - $125K/yr

Liaise with medical monitor and cross functional team members as necessary and in accordance with ... Minimum of 3 years of clinical trial experience, including prior experience in oncology clinical ...

Orion Group

$115 - $123/hr

The Medical Monitor / Medical Monitor Trainer leads the direction, planning, execution, and interpretation of clinical trial data for one or more early-phase clinical development programs, with ...

PROMETRIKA, LLC

Clinical Trial Manager

Cambridge, MA · On-site

Clinical Trial Manager PROMETRIKA is a full-service clinical research organization (CRO) with ... Collaborate with Pharmacovigilance and Medical Monitoring to ensure timely safety reporting, SAE ...

Cugene Inc.

Medical Monitor

Boston, MA · On-site

Role Description The Medical Monitor will provide medical leadership and oversight for early- to ... Strong clinical trial design and execution ability * Excellent written and verbal communication

New

Prometrika LLC

Clinical Trial Manager

Cambridge, MA · On-site

$140K - $168K/yr

Collaborate with Pharmacovigilance and Medical Monitoring to ensure timely safety reporting, SAE ... clinical trial operations * Demonstrated experience managing multiple studies, sites and vendors ...

Prometrika, Llc

Clinical Trial Manager

Cambridge, MA · On-site

$140 - $168/hr

Collaborate with Pharmacovigilance and Medical Monitoring to ensure timely safety reporting, SAE ... clinical trial operations * Demonstrated experience managing multiple studies, sites and vendors ...

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Medical Monitor Clinical Trial information

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How much do medical monitor clinical trial jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for medical monitor clinical trial in the United States is $37.67, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $48.08 per hour, depending on experience, location, and employer.

What is a medical monitor clinical trial?

A Medical Monitor in a clinical trial is a physician responsible for ensuring the safety of trial participants and the integrity of the study. They review and analyze clinical data, assess adverse events, and provide medical expertise to ensure compliance with regulatory and ethical guidelines. Medical Monitors collaborate with investigators, sponsors, and regulatory agencies to guide the trial's medical aspects. Their role is crucial in maintaining patient safety while ensuring the study's scientific and regulatory requirements are met.

What are the main daily responsibilities of a medical monitor in a clinical trial?

A Medical Monitor in a clinical trial is primarily responsible for overseeing participant safety and ensuring that the study is conducted in accordance with clinical protocols and regulatory standards. This involves reviewing and assessing adverse event reports, providing medical expertise to the clinical team, and communicating with investigators to resolve medical queries. You’ll also participate in safety data review meetings and contribute to key trial documents such as safety monitoring plans. The role requires ongoing collaboration with data management, regulatory, and pharmacovigilance teams to ensure a smooth and compliant trial process.

What are the key skills and qualifications needed to thrive in the medical monitor clinical trial position?

To thrive as a Medical Monitor Clinical Trial, you need an MD or equivalent medical degree, comprehensive clinical expertise, and experience with Good Clinical Practice (GCP) guidelines. Familiarity with clinical trial management systems, electronic data capture platforms, and relevant regulatory documentation is essential, as is certification such as Board Certification or GCP training. Strong analytical thinking, effective communication, and collaborative problem-solving skills make a candidate stand out in this role. These competencies are crucial to ensure participant safety, maintain regulatory compliance, and facilitate the success of clinical trials.

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Medical Monitor Clinical Trial jobs near you
Infographic showing various Medical Monitor Clinical Trial job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $78,347 per year, or $37.7 per hour.

Clinical Trial Manager

Verastem

Boston, MA • On-site

$100K - $125K/yr

Full-time

Re-posted 3 days ago

Job description

Summary:
We are seeking a Clinical Trial Manager with experience in managing a global Phase 3 clinical trial. Works with senior Clinical Operations members to lead the clinical project team members in the selection of vendors along with overseeing the completion of deliverables in a timely fashion within an agreed upon project budget. General areas of responsibility include: project planning, initiation, implementation, and closure; leading and motivating a cross functional team; milestone planning and tracking; ensuring that projects are progressing according to quality standards, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP) guidelines, and/or other guidelines to fulfill local regulations; production and review of key project progress reports; management of communications between the project team and CROs and ancillary vendors; and contract and financial management.
Responsibilities:
  • Function as primary liaison between clinical vendors (CRO, IRT, eTMF) and Verastem Oncology to ensure understanding of expectations and scope of work, quality and budget. Proactively recognize any changes in SOW and work with CRO to manage accruals and SOW changes.
  • Manage assigned clinical trials to ensure that studies are conducted efficiently, on time, within budget and in accordance with established SOPs and applicable regulatory requirements.
  • Provide oversight of all elements of the project lifecycle from initial set-up to close out including vendor performance, internal metrics, quality assurance checks and communication of trial status.
  • Work with Senior Clinical Operations member on RFPs for distribution to vendors, review proposals, coordinate bid defenses and internal discussions in selecting vendors to maximize savings.
  • Negotiate master service agreements, work orders, contracts, and amendments for sites/vendors.
  • Assist in developing study-specific feasibilities and participate in site selection.
  • Contribute to the writing and/or review of clinical documents such as Protocols, Informed Consent Forms, case report forms (CRFs) design and completion guidelines, and other study-related documents.
  • Liaise with medical monitor and cross functional team members as necessary and in accordance with established SOPs to produce study deliverables (e.g., clinical protocols, CRFs, informed consent templates, project management plan, data management plan, safety management plan, medical monitoring plan, clinical monitoring plan, pharmacy/lab manuals, clinical study reports etc.).
  • Work closely with Data Management to ensure ongoing data cleaning including review of data management metric, review of patient profiles and data listings.
  • Work with CRO and/or core team members to address issues and risks associated with achieving the study deliverables and develop risk mitigation plan.
  • Oversee monitoring activities at clinical CROs by reviewing monitoring visit reports, protocol deviations and CAPAs; attend co-monitoring visits as required.
  • Chair cross functional study team meetings and maintain meeting minutes and action items for team follow-up.
  • Regularly meet with Manager to discuss overall clinical trial(s) plans, update forecasting, and identify potential issues with recommended solutions.
  • Identify issues and implement solutions to ensure the project remains on track; recognize the need to seek assistance or inform senior management of specific issues.
  • Assume responsibility for setting up trial master file and ensuring the trial(s) is "audit ready" at all times.
  • Review, complete and ensure implementation of corrective action plans in conjunction with manager and quality assurance at vendor(s), and individual site(s) as applicable. May participate in internal/external study related audit(s).
  • Update assigned tracking spreadsheets on an ongoing basis.
  • Work with Finance to forecast budgets and reconcile monthly/quarterly actuals versus actuals.
  • Work with Quality Assurance to create and update clinical SOPs.

Qualifications:
  • Global Phase 3 clinical trial management experience
  • Minimum of 3 years of clinical trial experience, including prior experience in oncology clinical studies. BA/BS degree or equivalent in a scientific or health care field is required.
  • Excellent understanding of ICH, GCP and other applicable regulatory guidelines required.
  • Excellent verbal and written communication skills to effectively communicate with site staff, vendors and internal cross functional team members.
  • Ability to prioritize and multi- task.
  • Travel may be required.

The base salary range ($100K - $125K) provided reflects our current estimate of what we anticipate paying for this position. Your actual base salary will be based on several factors, including job-related skills, experience, internal equity, relevant education or training, location, and market dynamics. In addition, you will be eligible for an annual bonus, equity compensation, and a competitive benefits package.

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