Top 145 clinical study manager Jobs in boston, ma

Clinical Trial Manager
TransMedics, Inc. —Andover, MA
- $112,400 - $140,200 a year
- Full-time
- Bachelor of Science
- Office
- Analysis skills
- Employee stock purchase plan
- Disability insurance
Quick Apply
Clinical Trial Manager
Apogee Therapeutics —Boston, MA
- $145,000 - $160,000 a year
- Remote
- 5 years
- Office
- Bachelor's degree
- Health insurance
- Paid time off
Clinical Research Director
Sanofi EU —Cambridge, MA
- $206,250 - $343,750 a year
- Medicine
- English
- Analysis skills
- Parental leave
9d
Clinical Monitoring Manager
Apogee Therapeutics —Boston, MA
- $150,000 - $170,000 a year
- Remote
- Microsoft Excel
- Bachelor's degree
- Travel
- Health insurance
- Paid time off
Senior Clinical Trial Manager (CTM)
Praxis Precision Medicines, Inc. —Boston, MA
- $168,000 - $188,000 a year
- Email
- Remote
- 5 years
- Bachelor's degree
- Contracts
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Clinical Project Manager
Deciphera Pharmaceuticals —Waltham, MA
- $129,000 - $194,000 a year
- Full-time
- Remote
- 5 years
- Master's degree
- Bachelor's degree
- Health insurance
- Dental insurance
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Clinical Research Associate II
AbbVie —Boston, MA
- $84,500 - $162,000 a year
- Full-time
- Remote
- Nursing
- Mid-level
- Organizational skills
- Paid holidays
- Health insurance
Per Diem Clinical Clinical Investigation Tech Sleep Med
The Brigham and Women's Hospital, Inc. —Boston, MA
- $20.16 - $29.01 an hour
- Part-time
- Hybrid work
- Databases
- Analysis skills
- Bachelor's degree
- Opportunities for advancement
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Clinical Trial Assistant
Galderma —Boston, MA
- Mid-level
- Office
- Administrative experience
Senior Manager, Clinical Operations
Nuvalent, Inc. —Cambridge, MA
- $145,000 - $175,000 a year
- Remote
- 5 years
- Bachelor's degree
- Quality control
- Health insurance
- Dental insurance
Senior Manager, Clinical Quality Assurance
Deciphera Pharmaceuticals —Waltham, MA
- $138,000 - $190,000 a year
- Full-time
- Remote
- Bachelor's degree
- Travel
- Conflict management
- Health insurance
- Dental insurance
Quick Apply
Clinical Trial Manager
Seaport Therapeutics —Boston, MA
- $133,000 - $157,000 a year
- Bachelor of Science
- Office
- Bachelor's degree
11d
Senior Clinical Study Manager
Veranex, Inc. —Boston, MA
- $125,600 - $179,630 a year
- Full-time
- 5 years
- Bachelor's degree
- Contracts
Quick Apply
8d
Clinical QC Manager- Hybrid
Zai Lab (US) LLC —Cambridge, MA
- $140,000 - $160,000 a year
- Full-time
- Hybrid work
- 5 years
- Office
- Bachelor's degree
- Paid time off
- Parental leave
Quick Apply
Program Manager (Research)
Center for Women's Mental Health at MGH —Boston, MA
- $70,000 - $100,000 a year
- Full-time
- 3 years
- Bachelor's degree
- Psychology
- Commuter assistance
- Health savings account
Quick Apply
14d
Clinical Trial Manager
Kymera Therapeutics —Watertown, MA
- $115,000 - $200,000 a year
- Bachelor of Science
- HIPAA
- Bachelor's degree
Quick Apply
Clinical Trial Associate I
Prometrika LLC —Cambridge, MA
- $60,000 - $75,000 a year
- Full-time
- Writing skills
- Bachelor's degree
- Organizational skills
Quick Apply
Senior Clinical Trial Manager
Eight Sleep —Boston, MA
- $140,000 - $175,000 a year
- Full-time
- Hybrid work
- 3 years
- Bachelor's degree
- Doctor of Philosophy
- Dental insurance
- Vision insurance
Clinical Trial Associate (6-Month Contract)
CRISPR Therapeutics, Inc. —South Boston, MA
- $40 - $50 an hour
- Full-time
- Bachelor of Science
- Quality control
- SharePoint
Quick Apply
Clinical Data Manager
TScan Therapeutics —Waltham, MA
- $130,000 - $150,000 a year
- Full-time
- Hybrid work
- 5 years
- Senior level
- Leadership
Quick Apply

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Clinical Trial Manager

TransMedics, Inc. -
Andover, MA

Quick Apply

Job Details

Full-time
$112,400 - $140,200 a year

Benefits

Employee stock purchase plan
Disability insurance
Health insurance
Dental insurance
401(k)
Flexible spending account
Paid time off
Vision insurance
Pet insurance

Qualifications

Clinical program budget management
Managing healthcare project budgets
Project documentation
Adverse event reporting
Clinical incident reports
Employee relationship building
Contract management in healthcare
Clinical audit and monitoring
ICH guidelines
Clinical program monitoring
Project management in healthcare
Vendor communication
Clinical quality assurance standards
IRB compliance
Regulatory compliance analysis
Cross-functional collaboration
Clinical data analysis
Technical Proficiency
Project stakeholder communication
Cross-functional communication

Full Job Description

Job Description:

POSITION SUMMARY

This Clinical Trial Manager role is responsible for leading the end-to-end execution of clinical trials, ensuring studies are delivered on time, within budget, and in compliance with regulatory and corporate standards. The position oversees trial start-up, conduct, and close-out activities, while serving as a key point of coordination across investigational sites, cross-functional teams, and external partners. This individual drives study progress through proactive communication, meticulous planning, and effective management of timelines, documentation, and trial metrics, contributing to the successful delivery of high-quality clinical data.

RESPONSIBILITIES
This position is responsible for, but not limited to, the following:

Lead for the end-to-end clinical trial delivery
Manage trial start-up, conduct, and close-out activities according to industry and corporate standards with Director support
Manage clinical site interactions (including assistance with IRB/EC applications, contract negotiations, enrollment tracking, clinical trial material and clinical supply requests, issue resolution, etc.)
Prepare key clinical documents (e.g. protocols, informed consent, amendments, CRF’s, training materials, project plans, monitoring plans, data plans, statistical analysis plans, summary reports, annual reports, etc.)
Establish professional rapport and engage in frequent communication with investigational site personnel in order to keep study on-track
Track internal metrics, timelines and budgets
Communicate trial status to trial cross functional team
Prepare and present trial specific metrics and updates to Director, Program Managers and Senior Management
Participate in monitoring activities at clinical trial sites to assure adherence to GCP and ICH guidelines, regulatory requirements, SOPs, protocols and ensure that data is complete and accurate
In conjunction with data management personnel, gain understanding of planning, monitoring, and executing data analyses
Support applications and technical files as needed
Collaborate with project specific committees (e.g., DSMB, CEC)
Assist with preparation for investigators’ meetings
Work with vendors as needed
Travel up to 25% of the time
Perform other TransMedics tasks and duties as assigned/required.

MANAGEMENT RESPONSIBILITIES

This position will not have management responsibilities.

MINIMUM QUALIFICATIONS

7+ years of CRA, CTA or equivalent, with medical device experience CTM experience preferred
BA/BS in Science, Life Sciences or relevant field; or equivalent combination of education and experience
Experience interacting with sites, monitors, IRB’s, sponsors, vendors, clinical centers, and FDA
Experience screening and recruiting patients for studies
Knowledge of adverse event investigation, analysis and reporting procedures and standards
Proficiency with electronic data management systems
Familiarity with clinical budget planning and management
Coordinating external and internal documentation for clinical trials
Understanding of data collection methodologies
Familiarity with GCP, ICH, ISO and FDA regulatory requirements
Experience in coordinating multi-center global clinical trials
Ability to build collaborative relationships both internally and externally
Willing to be held accountable for deliverables
Must be highly organized and detail oriented
Proven ability to handle multiple projects and changing priorities
Must be results-driven and exhibit a sense of urgency
Clear and concise in verbal and written communication, fosters smooth flow of timely and relevant information
Strong initiative and positive attitude

As part of our long-term growth plans, TransMedics is excited to announce our plan to relocate our headquarters (HQ) to Somerville, MA by 2028. We chose this location because we believe it is a place where innovation will thrive. Our new state-of-the-art headquarters is designed to support collaboration, creativity, and discovery. We believe this will be a place where we can continue to do things few thought possible in organ transplantation to help patients. Specific timing and role impact may vary.

Every Organ Wasted is a Life Not Saved.

TransMedics, Inc. is a commercial-stage medical technology company transforming organ transplant therapy for patients worldwide. Our mission is to help save more patients’ lives by increasing access to viable donor organs for those who are awaiting an organ transplant. To accomplish this mission, we partner closely with transplant stakeholders worldwide and help expand their access to healthy donor organs, while delivering the highest quality technology, service, clinical care and outcomes.

Driven by a passion for improving patient care, we make the impossible possible and keep our employees at the center of everything we do. Together, we strive to enhance the quality of life for transplant recipients and their families, fostering hope and healing in the journey toward better health.

Maximize your potential at TransMedics, Inc.

www.TransMedics.com

TransMedics is committed to equitable and transparent compensation. The expected base salary range for this role is $112,400.00 – $140,200.00, which represents the company’s current good-faith estimate of compensation for this position. Actual salary will depend on factors such as, but not limited to, candidate experience, qualifications, skills, and the specific work location. This role may also be eligible for bonuses, equity, and a comprehensive benefits package (medical, dental, vision, retirement savings, paid time off, and wellness resources). We comply with all U.S. pay transparency laws and do not request or consider salary history.

Employee Benefit:

Medical with Health Reimbursement Account through Blue Cross/Blue Shield of MA

Dental

Vision

Healthcare Flexible Spending Account

Dependent Care Flexible Spending Account

Short Term Disability

Long Term Disability

401K Plan

Pet insurance

Employee Stock Purchase Plan

TransMedics is an equal opportunity employer and does not discriminate on the basis of race, color, religion, sex, national origin, marital status, age, disability or protected veteran status, or any other characteristic protected by law. We are committed to creating an inclusive environment for all employees.

Quick Apply

Refine Your Search

clinical study manager jobs in boston, ma

Clinical Trial Manager

Clinical Trial Manager

Clinical Research Director

Clinical Monitoring Manager

Senior Clinical Trial Manager (CTM)

Clinical Project Manager

Clinical Research Associate II

Per Diem Clinical Clinical Investigation Tech Sleep Med

Clinical Trial Assistant

Senior Manager, Clinical Operations

Senior Manager, Clinical Quality Assurance

Clinical Trial Manager

Senior Clinical Study Manager

Clinical QC Manager- Hybrid

Program Manager (Research)

Clinical Trial Manager

Clinical Trial Associate I

Senior Clinical Trial Manager

Clinical Trial Associate (6-Month Contract)

Clinical Data Manager

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