Top 397 Clinical research associate Jobs in Boston, Ma

Clinical Research Associate
Alira Health —Boston, MA
- $85,000 - $125,000 a year
- Full-time
- Bachelor of Science
- English
- Mid-level
8d
Clinical Research Assistant
Adams Clinical —Boston, MA
- $24.00 - $26.92 an hour
- Vital signs
- High school diploma or GED
- Bachelor's degree
- Health savings account
- Health insurance
1d
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
Clinical Research Associate
Alliance for Clinical Trial in Oncology Foundation —Boston, MA
- $57,000 - $75,000 a year
- Full-time
- Hybrid work
- Microsoft Excel
- Bachelor of Science
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Associate
The General Hospital Corporation —Boston, MA
- $20.16 - $29.01 an hour
- Full-time
- Bachelor's degree
- In-person
- Communication skills
- Opportunities for advancement
Quick Apply
7d
Research Associate
Eight Sleep —Boston, MA
- $70,000 - $100,000 a year
- Weekends as needed
- Computer Science
- HIPAA
- Mid-level
Clinical Trial Associate, Clinical Operations
Moderna, Inc. —Cambridge, MA
- $74,000 - $118,400 a year
- Full-time
- Mid-level
- Office
- Bachelor's degree
- Paid time off
- Adoption assistance
8d
Clinical Research Assistant Opportunities – Multiple Locations Nationwide
Headlands Research —Boston, MA
- Bachelor's degree
- Psychology
- Communication skills
Quick Apply
Senior Clinical Research Associate (level dependent on experience)
CTI Clinical Trial Services, Inc —Boston, MA
- Hybrid work
- Nursing
- Mid-level
- Master's degree
- Paid parental leave
- Tuition reimbursement
Quick Apply
Clinical Research Data Specialist I
Mass General Brigham Incorporated —Boston, MA
- $20.16 - $29.01 an hour
- Full-time
- Remote
- Vital signs
- Computer literacy
- Bachelor's degree
- Opportunities for advancement
Quick Apply
1d
Research Associate
Beth Israel Lahey Health —Boston, MA
- $27.00 - $38.46 an hour
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Hospital
Protocol Associate – Oncology Clinical Research
ECOG-ACRIN Medical Research Foundation —Boston, MA
- $50,000 - $70,000 a year
- Full-time
- Hybrid work
- Mid-level
- Office
- Bachelor's degree
- Health insurance
- Dental insurance
Quick Apply
1d
Clinical Trial Associate, Clinical Operations, Infectious Disease
Moderna, Inc. —Cambridge, MA
- $74,000 - $118,400 a year
- Full-time
- Mid-level
- Office
- Bachelor's degree
- Paid time off
- Adoption assistance
8d
Clinical Trial Associate, Clinical Operations, Therapeutics and Oncology
Moderna, Inc. —Cambridge, MA
- $74,000 - $118,400 a year
- Full-time
- Mid-level
- Office
- Bachelor's degree
- Paid time off
- Adoption assistance
12d
Clinical Research Assistant II
Beth Israel Lahey Health —Boston, MA
- $19.23 - $31.25 an hour
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Hospital
Associate Director, Clinical Quality Assurance
BioNTech AG —Cambridge, MA
- $163,000 - $200,000 a year
- Full-time
- Background check
- 5 years
- Mentoring
- Health savings account
- AD&D insurance
Region Manager
Care Access —Boston, MA
- $95,000 - $115,000 a year
- Up to 50% travel
- Inventory management
- Pass drug screening
- Health savings account
- Paid holidays
Associate Director, Clinical Operations Program Lead
Takeda Pharmaceutical —Boston, MA
- $154,400 - $242,550 a year
- Full-time
- Remote
- English
- Bachelor's degree
- Conflict management
- Paid holidays
- Disability insurance
Associate Director, Clinical Trial Reporting
Takeda Pharmaceutical —Boston, MA
- $154,400 - $242,550 a year
- Full-time
- Remote
- 6 years
- Bachelor of Science
- Bachelor's degree
- Paid holidays
- Disability insurance
Lead Clinical Study Manager
Takeda Pharmaceutical —Boston, MA
- $116,000 - $182,270 a year
- Full-time
- Remote
- 6 years
- Doctoral degree
- Bachelor of Science
- Paid holidays
- Disability insurance

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Clinical Research Associate

Alira Health -
Boston, MA

Apply Now

Job Details

Full-time
$85,000 - $125,000 a year
8 days ago

Qualifications

Employee relationship building
Bachelor's degree
Task prioritization

Full Job Description

Are you being referred to one of our roles by a connection in Alira Health? If so, please apply using the referral link emailed to you.

Join our global team dedicated to innovation and initiative, where physical walls and different time zones don’t limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is driven by our shared values: be courageous, be accountable, be honest, be inclusive and elevate others.

Job Description Summary

The CRA is an important member of the Alira Health Clinical team. The CRA is highly motivated and functions independently to conduct site monitoring responsibilities for clinical trials; as well as providing oversight, leadership, and guidance in the management and execution of clinical trials to ensure compliance and quality. The CRA works closely with Lead CRAs, Sr CRAs, in-house CRAs, Associate Director of Clinical Monitoring and Project Managers to ensure protocol compliance, address site questions, and assist with study recruitment, site training, and other site-related issues.

Job Description

KEY RESPONSABILITIES

Provides guidance, oversight, and feedback to the CRA team to ensure adherence to project scope, SOPs, timelines, and budget requirements.
Reviews monitoring visit reports, conducts co-monitoring and evaluation visits as needed.
Ensures appropriate and timely investigator site visits.
Coordinates with appropriate cross-functional departments to facilitate negotiation/issue resolution for clinical trial monitoring related issues.
Assists in development of study-specific Monitoring Plans and training presentations as required.
Assists in set up/collection of site specific ethics documents and site contract negotiation as required.
Provides monthly billing information to finance team as required.
For monitoring stand-alone projects, manages study budget and acts as referent for the sponsor.
Performs qualification, initiation, interim, and close-out visits both remotely and onsite, ensuring proper documentation of monitoring visits.
Prepares consistently accurate and timely monitoring visit reports documenting site-related problems, resolutions, actions taken, protocol deviations, study progress, and enrollment status.
Ensures integrity of CRF data through meticulous and thorough source document review and verification.
Performs quality control and verification of documents collected at sites for eTMF/TMF.
Conducts investigational product accountability.
Reviews site regulatory binder for required documents.
Maintains regular contact with study sites to ensure protocol/GCP compliance, assesses patient accrual rates, and responds to sponsor requests.
Complies with and ensures team compliance with ICH GCP guidelines, FDA regulations, and company/Sponsor SOPs.
Participates in internal, client/sponsor, scientific, and other meetings as required.
Facilitates adverse event reporting and ensures the reconciliation of SAE reports with source documentation and CRFs.
Works closely with in-house CRAs/CTC and data management to resolve queries on discrepant data.
Proactively identifies site issues and develops problem-solving strategies for sites.
Conducts audit preparation at study sites as needed.
Works with other CRAs to maintain consistency and promote a collaborative team atmosphere.
Participates in internal, client/sponsor, scientific, and other meetings as required.
Assists in CRA new hire training and onboarding.
Performs CRA mentoring.
Collaborates with development and maintenance of Clinical Trial Management System (CTMS).
Manages and resolves conflicting priorities to deliver on commitments.
Performs additional duties as assigned.

Compensation: $85,000 - 125,000 commensurate with experience

DESIRED QUALIFICATION & EXPERIENCE

EU: Graduation in a scientific health field
EU (Italy): Certified Monitor in compliance with Italian CRO decree dated 15Nov2011
Ability to establish and maintain positive relationships with Sponsor, Site and Project Team members
Ability to autonomously manage monitoring activities

TECHNICAL COMPETENCES & SOFT SKILLS

Quality focused; Proven ability to be careful, thorough, and detail-oriented
Strong organizational skills and the ability to multi-task and work effectively in a fast-paced environment
Able to manage priorities, organize time and solve problems
Strong analytical, negotiation, meeting management, cross-functional team, and leadership skills
Ability to travel
Ability to manage stress
Professional, trustworthy and disciplined
Ability to problem-solve unstructured or ambiguous challenges
Strong command of Local language, both written and verbal, in the country where monitoring activities are performed
Excellent communication and interpersonal skills with customer service orientation
Good computer skills, with ability to use clinical trial management systems, clinical trial databases and electronic data capture
Self-starter who thrives in a collaborative, yet less structured team environment
Knowledge of clinical research, ICH GCP and local regulations
Knowledge of Regulatory and Ethical requirements
EU: Adequate English

Languages

English

Education

Bachelor of Science (BS): Biology, Bachelor of Science (BS): Life Sciences

Contract Type

Regular

Salary Range

The final offer will be determined within the applicable location-specific range and will depend on the candidate’s confirmed work location, relevant experience, skills, qualifications, internal equity, and role scope.

Apply Now

Refine Your Search

clinical research associate jobs in boston, ma

Clinical Research Associate

Clinical Research Assistant

Clinical Research Associate II

Clinical Research Associate

Clinical Research Associate

Research Associate

Clinical Trial Associate, Clinical Operations

Clinical Research Assistant Opportunities – Multiple Locations Nationwide

Senior Clinical Research Associate (level dependent on experience)

Clinical Research Data Specialist I

Research Associate

Protocol Associate – Oncology Clinical Research

Clinical Trial Associate, Clinical Operations, Infectious Disease

Clinical Trial Associate, Clinical Operations, Therapeutics and Oncology

Clinical Research Assistant II

Associate Director, Clinical Quality Assurance

Region Manager

Associate Director, Clinical Operations Program Lead

Associate Director, Clinical Trial Reporting

Lead Clinical Study Manager

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