Sr. Clinical Research Associate

Getinge; Waltham (MA); On-site; USD 110,000 - 125,000; Full time

Benefits offered by this job

Health insurance

401k plan

Paid Time Off

Tuition reimbursement

Job summary

Getinge is seeking a Senior Clinical Research Associate to oversee randomized clinical studies across solid organ platforms. The role reports to the VP Scientific and Medical Affairs and focuses on data management, site coordination, and ensuring GCP compliance.

The position requires 6+ years in clinical research, a Bachelor's degree, and willingness to travel up to 20%. The role supports diverse teams and contributes to high-quality study deliverables.

Qualifications

• Bachelor's degree in health sciences or related field
• Minimum 6+ years of clinical research associate experience, including randomized trials in medical devices or pharma
• Experience in cardiothoracic clinical trials preferred

Responsibilities

• Provides data coordination and data management for randomized clinical studies.
• Manages investigative site activity for multiple protocols.
• Coordinates budgets and invoicing.
• Creates and implements subject enrollment strategies for assigned sites.
• Ensures trials are conducted per ICH GCP, regulations, and SOPs.
• Designs CRFs/eCRFs for data collection and entry.
• Trains sites on data capture and data cleaning; supports data corrections.

Skills

Data coordination

Data management

Clinical research

Budget coordination

Site management

Travel readiness

Education

Bachelor's degree

Tools

CRF/eCRF design

Data capture tools

Job description

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Sr. Clinical Research Associate

Date: Aug 14, 2026

Location: Waltham, MA, US

Company: Paragonix Technologies, Inc.

Remote Work: 1-2 days at home (site based)

Salary Range: The minimum base salary for this position is $110,

With a passion for life

Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people. To make a true difference for our customers - and to save more lives, we need team players, forward thinkers, and game changers.

Are you looking for an inspiring career? You just found it.

This role is open to US based candidates

Paragonix Technologies develops and markets organ transportation and preservation devices that safeguard organs during the journey between donor and recipient patients. Our devices incorporate clinically proven and medically trusted cold preservation techniques in a novel suspension system to provide unprecedented physical and thermal protection. Our product portfolio spans cardiac, thoracic, and abdominal preservation devices to improve donor organ quality and extend donor organ transport time.

Position Overview:

The Senior Clinical Research Associate is responsible for oversight of the prospective randomized clinical studies conducted by Paragonix Technologies. This position is responsible for managing studies across solid organ platforms. The Senior Clinical Research Associate will report to the VP Scientific and Medical Affairs and will play an important role in study data management and overall clinical operations of the prospective randomized studies.

Job Responsibilities and Essential Duties

• Provides data coordination and data management for randomized clinical studies.
• Manages investigative site activity for multiple protocols.
• Coordinates budgets and invoicing
• Creates and implements subject enrollment strategies for assigned investigative sites.
• Ensures clinical trials are managed and executed following ICH GCP, regulations, the protocol, and company-specific SOPs.
• Designs CRFs and eCRFs for data acquisition and data entry.
• Works closely with sites to train and support data capture and cleaning, coordinating efficient corrections to the database, assisting with troubleshooting and site challenges.
• Defining necessary validations or reports to ensure quality and timeliness of data collection.
• Monitoring study metrics and site performance using standard study management tools.
• Collaborates with the study team to prepare abstracts, manuscripts, and other materials for internal and external audiences.
• Participates in meetings with multidisciplinary teams both internally and externally to ensure successful and timely completion of deliverables.
• Supports reporting to clinicaltrials.gov including data review, quality control checks, and interim and final analysis.
• Ability to understand the objectives of a study and ensure that the databases, study case report forms, and data analysis match the overall study goals.

Required Knowledge & Skills

• Minimum requirement of a Bachelor's Degree, preferably in health sciences or a related field
• Minimum of 6+ years of clinical research associate experience, in particular in supporting randomized clinical trials in either the medical device or pharmaceutical industry is required.
• Experience in cardiothoracic clinical trials preferred.

Other Requirements:

• Experience with data collection and project management tools.
• Critical attention to detail and accuracy.
• Ability to communicate appropriately and effectively both orally and in writing.
• Must be willing to travel domestically/internationally 1% - 20%.

US BASED SALARY - The minimum base salary for this position is $110,000 and the maximum salary is $125,000 plus 10% in annual bonus

About us

With a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. The offering includes products and solutions for intensive care, cardiovascular procedures, operating rooms, sterile reprocessing and life science. Getinge employs over 12,000 people worldwide and the products are sold in more than 135 countries.

Benefits at Getinge:

At Getinge, we offer a comprehensive benefits package, which includes:

• Health, Dental, and Vision insurance benefits
• 401k plan with company match
• Paid Time Off
• Wellness initiative & Health Assistance Resources
• Life Insurance
• Short and Long Term Disability Benefits
• Health and Dependent Care Flexible Spending Accounts
• Parental and Caregiver Leave
• Tuition Reimbursement

Getinge is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, pregnancy, genetic information, national origin, disability, protected veteran status or any other characteristic protected by law.Reasonable accommodations are available upon request for candidates taking part in all aspects of the selection process.