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Entry Level Clinical Research Associate Jobs in Sharon, MA

Getinge

Sr. Clinical Research Associate

Boston, MA · On-site

$125K/yr

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 ...

Getinge

Sr. Clinical Research Associate

Boston, MA · Hybrid

$125K/yr

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 ...

Icon plc

Clinical Research Associate II

Cambridge, MA · Remote

Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements. * Proven ability to manage multiple sites and projects ...

Icon plc

Clinical Research Associate II

Boston, MA · Remote

Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements. * Proven ability to manage multiple sites and projects ...

Alira Health

Clinical Research Associate

Framingham, MA · On-site

Summary ROLE The Clinical Research Associate is an important member of the Alira Health Clinical team. CRAs are highly motivated and function independently to conduct site monitoring responsibilities ...

Massgeneralbrigham

Clinical Research Associate

Boston, MA · Remote

$20.16 - $29.01/hr

The CRRCI will be trained on the institutional and federal regulations governing clinical research. Essential Functions: -Maintain and organize study-specific regulatory binders. -Prepare and submit ...

Mass General Brigham

Clinical Research Associate

Boston, MA · On-site +1

$20.16 - $29.01/hr

The CRRCI will be trained on the institutional and federal regulations governing clinical research. Essential Functions: -Maintain and organize study-specific regulatory binders. -Prepare and submit ...

Adams Clinical

Clinical Research Assistant

Boston, MA · On-site

$24 - $26.92/hr

This role is ideal for entry-level candidates interested in learning clinical research operations, contributing to study execution, and developing foundational skills in patient interaction, data ...

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Entry Level Clinical Research Associate information

What is an entry level clinical research associate?

An Entry Level Clinical Research Associate (CRA) is responsible for monitoring clinical trials to ensure compliance with regulatory requirements, ethical guidelines, and study protocols. They assist in site selection, data collection, and verifying that study procedures are properly followed. Entry-level CRAs typically work under the supervision of senior CRAs and may travel to different clinical sites. Strong attention to detail, knowledge of Good Clinical Practice (GCP) guidelines, and organizational skills are essential. This role is a starting point for a career in clinical research, with opportunities for growth into senior CRA or project management positions.

What are the typical daily responsibilities of an entry level clinical research associate?

As an Entry Level Clinical Research Associate, your day-to-day work generally involves assisting with monitoring clinical trial sites, reviewing study documentation, and ensuring adherence to protocol and regulatory requirements. You may support more senior team members in conducting on-site or remote visits, tracking patient recruitment, and managing data collection. Additionally, you’ll communicate regularly with site staff and other stakeholders to resolve issues and ensure data quality. This hands-on experience is essential for building expertise in clinical research processes and advancing toward more senior CRA roles.

What are the key skills and qualifications needed to thrive as an entry level clinical research associate?

To thrive as an Entry Level Clinical Research Associate, you typically need a bachelor's degree in life sciences or a related field, a solid understanding of clinical trial protocols, and attention to detail. Familiarity with Good Clinical Practice (GCP) guidelines, electronic data capture (EDC) systems, and regulatory documentation is often required. Strong communication, organization, and problem-solving abilities help you effectively collaborate with study sites and team members. These skills are critical to ensure the accuracy, compliance, and successful progression of clinical studies.

What job categories do people searching Entry Level Clinical Research Associate jobs in Sharon, MA look for?

The top searched job categories for Entry Level Clinical Research Associate jobs in Sharon, MA are:

What cities near Sharon, MA are hiring for Entry Level Clinical Research Associate jobs?

Cities near Sharon, MA with the most Entry Level Clinical Research Associate job openings:

Entry Level Clinical Research Associate jobs near you
Infographic showing various Entry Level Clinical Research Associate job openings in Sharon, MA as of August 2026, with employment types broken down into 2% As Needed, 77% Full Time, 15% Part Time, and 6% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution.

Sr. Clinical Research Associate

Getinge

Boston, MA • On-site

$125K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 8 days ago

Getinge rating

9.3

Company rating: 9.3 out of 10

Based on 14 frontline employees who took The Breakroom Quiz

12th of 495 rated machine equipment manufacturers

Job description

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
#LI-YA2 #LI-Hybrid
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
  • Commuter Benefits
  • 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.

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About Getinge

Sourced by ZipRecruiter

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Dr Wayne, NJ, US

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