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Clinical Study Manager Jobs in Reading, MA (NOW HIRING)

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Clinical Study Specialist

Cambridge, MA · Hybrid

$62K - $77K/yr

Clinical Study Specialist (Hybrid - Warren, NJ, Armonk, NY or Cambridge MA)) ICON is a global ... Manages and maintains team SharePoint and/or shared drive sites, as needed * Communication with ...

RadNet

Senior Clinical Studies Associate

Somerville, MA · On-site

$71K - $96K/yr

Working under the guidance of Clinical Study Manager and cross-functional study teams, the SCSA contributes to study operations, documentation, regulatory compliance, and process improvement ...

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Clinical Study Lead

Boston, MA · Hybrid

$121K - $151K/yr

Clinical Study Lead ICON is a global healthcare intelligence and clinical research organisation ... Coordinates & manages various tasks in collaboration with other sponsor roles to achieve site ...

410 ICR United States USA

Clinical Study Lead

Boston, MA · Hybrid

$121K - $151K/yr

Clinical Study Lead ICON is a global healthcare intelligence and clinical research organisation ... Coordinates & manages various tasks in collaboration with other sponsor roles to achieve site ...

ARTBIO

Senior Clinical Trial Manager

Cambridge, MA · On-site

Drive study startup activities, including feasibility, site selection, and timelines. * Manage activities of Phase 1 and 2 clinical trial investigators with a focus on the US to ensure compliance ...

ARTBIO

Senior Clinical Trial Manager

Cambridge, MA · On-site +1

Drive study startup activities, including feasibility, site selection, and timelines. * Manage activities of Phase 1 and 2 clinical trial investigators with a focus on the US to ensure compliance ...

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All JobsClinical Study JobsClinical Study Manager JobsClinical Study Manager Jobs in Reading, MA

Clinical Study Manager information

See Reading, MA salary details

$30

$65

$101

How much do clinical study manager jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for clinical study manager in Reading, MA is $65.97, according to ZipRecruiter salary data. Most workers in this role earn between $53.51 and $74.33 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a clinical study manager?

To thrive as a Clinical Study Manager, you need a strong background in clinical research, project management, and regulatory compliance, typically supported by a degree in life sciences and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications like GCP (Good Clinical Practice) are highly valued. Strong organizational, leadership, and communication skills help manage cross-functional teams and ensure study timelines are met. These skills are crucial for maintaining study quality, ensuring regulatory adherence, and delivering successful trial outcomes.

What are some common challenges faced by clinical study managers, and how can they be addressed?

Clinical Study Managers often encounter challenges such as coordinating multiple stakeholders, ensuring regulatory compliance, and managing tight timelines across study sites. Effective communication and proactive planning are essential to address these issues, as well as staying up to date with changing industry regulations. Building strong relationships with site staff and fostering a collaborative team environment can also help mitigate delays and ensure study milestones are met successfully.

How much does a clinical study manager earn?

A clinical study manager's salary varies based on experience, location, and the size of the organization, but typically ranges from $80,000 to $130,000 annually. Senior roles or those with specialized skills and certifications can earn higher salaries, often exceeding $150,000. The position often requires knowledge of regulatory guidelines and project management tools.

What does a clinical study manager do?

A clinical study manager oversees the planning, execution, and monitoring of clinical trials to ensure they comply with regulatory standards and protocols. They coordinate with research teams, manage timelines and budgets, and ensure data quality, often using specialized software and requiring knowledge of Good Clinical Practice (GCP) guidelines.

What job categories do people searching Clinical Study Manager jobs in Reading, MA look for?

The top searched job categories for Clinical Study Manager jobs in Reading, MA are:

What cities near Reading, MA are hiring for Clinical Study Manager jobs?

Cities near Reading, MA with the most Clinical Study Manager job openings:

Clinical Study Manager jobs near you
Infographic showing various Clinical Study Manager job openings in Reading, MA as of August 2026, with employment types broken down into 83% Full Time, 15% Part Time, 1% Temporary, and 1% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $137,211 per year, or $66 per hour.

Clinical Study Operations Manager

Beacon Biosignals

Boston, MA • On-site, Remote

$90K - $110K/yr

Full-time, Contractor

PTO

Posted 22 days ago

Job description

As a Clinical Study Operations Manager within the Clinical Study Operations team, you will be responsible for ensuring the successful operational delivery of Beacon's clinical studies, from startup through close-out. You will work closely with sponsors, project teams, and clinical sites to drive efficient study execution and uphold Beacon's commitment to quality, compliance, and scientific rigor.
 
You will oversee study startup planning, site onboarding and training, and ongoing operational oversight to ensure studies are executed on time and to the highest standards. Acting as a key operational partner to both sponsors and internal teams, you will proactively identify risks, streamline communication, and maintain alignment across stakeholders. In addition, you will foster a culture of quality within the organization by coaching peers on GCP compliance, documentation discipline, version control, and complaint management, strengthening the team's collective operational excellence.
 
This is a contract-to-hire individual contributor role, fully remote anywhere in the U.S., and will require up to 10% travel. Beacon's robust asynchronous work practices ensure a first-class remote work experience, but we also have in-person office hubs available located in Boston, New York and Paris.
 
What success looks like:
  • Collaborate with project teams to implement study startup activities, including communication planning, logistics, development of study documentation, and data configuration.
  • Instill confidence with clients on study operations through start up, maintenance and close out activities.
  • Act as the primary point of contact for clinical sites, ensuring smooth operations and clear communication.
  • Provide training to research sites on the use of Beacon's devices and study protocols, ensuring proper device usage and data collection.
  • Monitor project progress, ensuring adherence to timelines, protocols, and quality standards.
  • Maintain compliance with Good Clinical Practice (GCP), International Conference on Harmonization (ICH) guidelines, and regulatory standards.
  • Foster a culture of quality within the ClinOps and Scientific teams by coaching peers on GCP requirements, documentation discipline, versioning, and complaint management.
  • Address operational issues promptly, escalating through tools like Zendesk and Asana for resolution.
  • Provide actionable feedback from research sites to inform improvements in devices and workflows.
 
What you will bring:
  • 5+ years of experience in clinical project management or clinical operations roles.
  • Strong organizational and project management skills, with the ability to manage multiple responsibilities effectively.
  • Excellent written and verbal communication skills in English; additional languages are a bonus.
  • A proactive mindset with the ability to identify priorities and anticipate challenges.
  • Meticulous attention to detail, ensuring accuracy in data collection and reporting.
  • Ability to work in a fast paced environment with multiple priorities.
  • Familiarity with GCP, ICH guidelines, and clinical research regulatory requirements.
  • Knowledge of decentralized data collection, compliance and oversight while showing empathy for both patients and sites.
  • A desire to learn more about analytics, statistics, machine learning, and clinical trials.
The salary range for this role is $90,000 - $110,000. Salary ranges are determined using current market compensation data for this role and adjusted based on experience, skills, and location. The base salary is one component of the total compensation package, which includes equity, PTO and other benefits.
 
At Beacon, we've found that cultural and scientific impact is driven most by those that lead by example. As such, we're always seeking new contributors whose work demonstrates an avid curiosity, a bias towards simplicity, an eye for composability, a self-service mindset, and - most of all - a deep empathy towards colleagues, stakeholders, users, and patients. We believe a diverse team builds more robust systems and achieves higher impact.

Apply