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Clinical Operation Associate Jobs in Walpole, MA

Vor Bio

Associate Director Clinical Operations

Boston, MA · On-site

  • Medical

  • Retirement

  • PTO

Vor Biopharma is seeking an Associate Director of Clinical Operations to manage our autoimmune programs. The ideal candidate will initiate and lead clinical trials across all phases, including ...

System One

Associate Director Clinical Operations

Waltham, MA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Associate Director Clinical Operations Location: Waltham, Massachusetts Type: Perm Work Model: Hybrid - 2 days onsite in Waltham Leading Pharmaceutical Company located in MA is hiring a Associate ...

System One

Associate Director Clinical Operations

Waltham, MA · Remote

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Associate Director Clinical Operations Location: Waltham, Massachusetts Type: Permanent Work Model: Hybrid - onsite and remote This Associate Director, Clinical Operations role is a key leadership ...

System One

Associate Director Clinical Operations

Waltham, MA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Associate Director Clinical Operations Location: Waltham, Massachusetts Type: Perm Work Model: Hybrid - 2 days onsite in Waltham Leading Pharmaceutical Company located in MA is hiring a Associate ...

System One

Associate Director Clinical Operations

Waltham, MA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Associate Director Clinical Operations Location: Waltham, Massachusetts Type: Perm Work Model: Hybrid - 2 days onsite in Waltham Leading Pharmaceutical Company located in MA is hiring a Associate ...

System One

Associate Director Clinical Operations

Waltham, MA · Remote

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Associate Director Clinical Operations Location: Waltham, Massachusetts Type: Perm Work Model: Hybrid - onsite and remote Leading Pharmaceutical Company located in MA is hiring a Associate Director ...

System One

Associate Director Clinical Operations

Waltham, MA · Remote

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Associate Director Clinical Operations Location: Waltham, Massachusetts Type: Permanent Work Model: Hybrid - onsite and remote This Associate Director, Clinical Operations role is a key leadership ...

Adams Clinical

Senior Manager, Clinical Operations

Boston, MA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Work closely with the Inpatient Unit Manager and the Associate Director of Inpatient Clinical Operations to support and oversee the conduct and quality of all inpatient studies at the Watertown ...

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All JobsClinical Operation Associate JobsClinical Operation Associate Jobs in Walpole, MA

Clinical Operation Associate information

See Walpole, MA salary details

$13

$34

$60

How much do clinical operation associate jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for clinical operation associate in Walpole, MA is $34.39, according to ZipRecruiter salary data. Most workers in this role earn between $23.08 and $45.34 per hour, depending on experience, location, and employer.

What is a clinical operation associate?

Clinical Operation Associates are professionals who support the planning, coordination, and execution of clinical trials within pharmaceutical, biotechnology, or clinical research organizations. They help ensure that clinical studies adhere to regulatory guidelines, timelines, and quality standards. Their responsibilities often include documentation management, assisting with trial site communications, tracking study progress, and supporting the clinical operations team with administrative tasks. Clinical Operation Associates play a vital role in the smooth running of clinical trials, contributing to the development of new medical treatments.

What are the key skills and qualifications needed to thrive as a clinical operation associate?

To thrive as a Clinical Operation Associate, you need a solid understanding of clinical trial processes, regulatory guidelines, and a relevant degree in life sciences or a health-related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC), and basic project management tools is typically required. Strong organizational skills, attention to detail, and effective communication are standout soft skills in this role. These capabilities ensure regulatory compliance, efficient trial execution, and seamless coordination among stakeholders in clinical research settings.

What are some common challenges clinical operation associates face when coordinating clinical trials, and how can they be managed?

Clinical Operation Associates often encounter challenges such as managing tight timelines, ensuring regulatory compliance, and coordinating communication among diverse stakeholders. Balancing multiple study sites and adapting to protocol amendments can also add complexity. Effective organization, proactive communication, and a strong understanding of clinical trial processes are key to overcoming these hurdles. Collaborating closely with site staff, clinical monitors, and project managers helps ensure that issues are identified early and addressed promptly, contributing to smoother trial operations.

What cities near Walpole, MA are hiring for Clinical Operation Associate jobs?

Cities near Walpole, MA with the most Clinical Operation Associate job openings:

Clinical Operation Associate jobs near you
Infographic showing various Clinical Operation Associate job openings in Walpole, MA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $71,528 per year, or $34.4 per hour.

Associate Director, Clinical Operations

Clinical Dynamix, Inc.

Watertown, MA

Full-time

Re-posted 8 days ago

Job description

Associate Director, Clinical Operations Job Description

How you’ll make an impact:

  • Contribute to the planning, implementation, and execution of global clinical trials.
  • Plan, execute, and lead study-specific meetings (e.g., internal core team meetings, investigator meetings, etc), as needed.
  • Provide input for the design of the Informed Consent Form(s), eCRFs, monitoring conventions, edit checks, etc.
  • Provide study-specific training and leadership to clinical research staff, CRO, CRAs, sites and other contract personnel.
  • Manage study timelines and metrics to ensure completion of study deliverables.
  • Lead site feasibility and selection qualification, initiation, and oversight of outsourced monitoring activities.
  • Review monitoring reports to ensure quality and resolution of site-related issues.
  • Ensure timely enrollment and data collection at clinical trial sites.
  • Collaborate with the data management team to ensure data integrity and timely database lock.
  • Ensure tracking, review of protocol deviations, and assess impact on study data.
  • Work closely with translational medicine team to ensure appropriate incorporation of bioanalytical sampling plan into clinical protocols and relevant data output of the trial is provided to functional groups for review.
  • Partner with Operational Excellence and assigned Site Engagement Leads to help drive site engagement and bolster recruitment
  • Serve as key counterpart of Clinical Outsourcing to build RFPs and support the selection of clinical vendors
  • Oversee and contribute to Sponsor Oversight activities including but not limited to review of KPIs, KRIs, PDs, risks, Data Review Findings, etc. to assess the health of the study and proactively ensure mitigations are in place to achieve Company’s quality standards
  • Contribute to clinical operations process improvement initiatives
  • Maintain accurate and complete trial documentation.
  • Proactively identify and resolve clinical project issues.
  • This role may require up to 25% travel

Skills and experience you’ll bring:

  • BS degree and 8+ years of experience in clinical operations in biotech/pharma. 5 years’ experience leading global clinical trials
  • Inspection readiness experience preferred
  • Experience working on large, global, complex phase 2b/3 or late stage trials. Respiratory or Immunology experience highly preferred.
  • Broad knowledge of Global regulations and guidelines including CFR, ICH GCP, HIPAA, GDPR, and the Protection of Human Research Subjects.
  • Strong project management skills with the ability to manage multiple trials simultaneously.
  • Excellent problem-solving, leadership, and communication skills.
  • Ability to work in a fast-paced, dynamic environment with cross-functional teams.