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Contract Cra Jobs in Needham, MA (NOW HIRING)

Summary The CRA is an important member of the Alira Health Clinical team. The CRA is highly ... Assists in set up/collection of site specific ethics documents and site contract negotiation as ...

Summary**The CRA is an important member of the Alira Health Clinical team. The CRA is highly ... Assists in set up/collection of site specific ethics documents and site contract negotiation as ...

... CRA team regarding project scope, SOPs, timelines, and budgets * • Review monitoring visit ... contract negotiation * • Provide monthly billing information to Finance * • Manage study ...

New

This role requires a detail-oriented and collaborative CRA who can independently manage assigned ... contract period. This is a 6 month, temporary position with an hourly pay rate of $45/hr.

Fire Protection Engineer

Worcester, MA · On-site

$73K - $132K/yr

... Support Contract (NISC) team. This role is for someone with experience in Fire Life Safety/Fire ... FLS Condition Risk Assessments (CRA): * Conduct comprehensive fire protection and life safety ...

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Contract Cra information

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$13

$44

$75

How much do contract cra jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for contract cra in Needham, MA is $44.80, according to ZipRecruiter salary data. Most workers in this role earn between $31.44 and $57.36 per hour, depending on experience, location, and employer.

What is a contract CRA?

A contract clinical research associate (contract CRA) is a temporary position in which you manage clinical trials and scientific research projects. As a contractor, you work temporarily on a contract that typically lasts for the duration of the project. Clinical research associates work in the pharmaceutical industry to ensure the safety and effectiveness of medication or vaccines. You can also work on studies for biotech companies and projects that perform analysis on surgical procedures or treatments. Your duties focus on planning the trial, defining the parameters, ensuring the safety of participants, and making sure the project meets all regulations and requirements.

What are the key skills and qualifications needed to thrive as a contract CRA, and why are they important?

To thrive as a Contract CRA, you need a solid understanding of clinical research protocols, regulatory guidelines (like GCP/ICH), and typically a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and sometimes certifications like ACRP or SOCRA are beneficial. Strong attention to detail, excellent organizational skills, and effective communication are crucial soft skills for managing multiple studies and collaborating with sites. These competencies are essential for ensuring compliance, data integrity, and the smooth execution of clinical trials.

What are some common challenges faced by contract CRAs and how can they effectively manage them?

Contract CRAs often juggle multiple clinical trial sites and studies, which can make prioritizing and time management especially challenging. They must adapt quickly to each sponsor's protocols and systems, often with limited onboarding. Building strong relationships with site staff and maintaining clear, consistent communication are key to overcoming these challenges. Staying organized through meticulous documentation and leveraging digital tools can help contract CRAs efficiently meet monitoring visit deadlines and regulatory requirements.

What job categories do people searching Contract Cra jobs in Needham, MA look for?

The top searched job categories for Contract Cra jobs in Needham, MA are:

What cities near Needham, MA are hiring for Contract Cra jobs?

Cities near Needham, MA with the most Contract Cra job openings:

Clinical Research Associate (CRA) - Temporary 6 Month Contract

Lighthouse Lab Services

Waltham, MA • On-site

$45/hr

Contractor, Temporary

Posted 24 days ago


Job description

 

Clinical Research Associate (CRA) – Temporary

Location: Waltham, MA
Schedule: Flexible hours, about 20 hours a week
Employment Type: 6 month-1 year Temporary/Contract

Pay Rate: $45/hour

Position Overview

Lighthouse Lab Services is seeking an experienced Clinical Research Associate (CRA) for a temporary opportunity in Waltham, MA. The Clinical Research Associate will be responsible for monitoring clinical studies and ensuring study execution is conducted in accordance with applicable laws, Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), and company standards.

The CRA will serve as a primary point of contact for assigned clinical partners and investigator sites, supporting study enrollment, monitoring, data quality, protocol compliance, and study close-out activities. This position will work closely with Regulatory Affairs and other members of the clinical study team to ensure studies are completed on time and to the required quality standards.

Responsibilities

  • Ensure proper conduct of clinical studies in accordance with SOPs, applicable laws, ICH/GCP guidelines, FDA regulations, and company standards.
  • Manage assigned operational aspects of clinical studies from study start through database lock, ensuring timelines and quality deliverables are met.
  • Serve as the primary point of contact for assigned clinical partners and investigator sites during study conduct.
  • Facilitate communication and information flow between clinical partners, investigators, vendors, and internal study team members.
  • Attend investigator meetings, either virtually or in person, as required.
  • Support patient enrollment and recruitment initiatives by identifying and addressing recruitment challenges with investigator sites.
  • Conduct remote/electronic monitoring activities and study close-out activities as needed.
  • Ensure monitoring activities are conducted in accordance with SOPs and are appropriately adjusted based on emerging study issues and technologies.
  • Monitor adverse events (AEs) and serious adverse events (SAEs), working with the study team to resolve outstanding issues and ensure required information is documented.
  • Maintain accurate and timely Trial Master File (TMF) documentation and study records.
  • Track and submit required reports, documentation, updates, and metrics, including protocol deviations, patient recruitment, clinical supplies, and overall study progress.
  • Resolve data queries and ensure close-out activities are completed within established timelines.
  • Ensure appropriate oversight of investigational products, including receipt, handling, accountability, storage conditions, and destruction.
  • Support database release activities as needed.
  • May perform responsibilities associated with an unblinded monitor when appropriate.
  • Collaborate with the Regulatory Affairs Manager and other study team members on study start-up, execution, and close-out activities.
  • Identify and resolve protocol-related issues to support successful study execution.

Qualifications

  • Bachelor's degree in a life science or related field, or a professional degree such as nursing, pharmacy, medicine, or equivalent.
  • Minimum of 3 years of relevant clinical research experience, including site monitoring experience.
  • Oncology clinical research experience preferred, with approximately 2 years of oncology monitoring experience strongly preferred.
  • Extensive knowledge of clinical study methodologies, ICH/GCP guidelines, and FDA regulations.
  • Experience with clinical site monitoring, study documentation, and clinical trial operations.
  • Strong organizational, communication, and problem-solving skills.
  • Fluent in English.
  • Valid driver's license required.

About us:

At Lighthouse Lab Services, we offer solutions to help start, grow, and run clinical laboratories. Our recruiting team has over 21 years of proven success placing job seekers in positions ranging from entry-level Medical Technologists to seasoned Laboratory Directors. We recruit nationwide, for permanent and travel positions with clients ranging from small hospitals to large reference laboratories.
It is the policy of Lighthouse Lab Services to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. Lighthouse Lab Services is committed to working and providing reasonable accommodation to individuals of all abilities, including persons with disabilities.
If at any time during the application process, you need an accommodation, please contact recruiting@lighthouselabservices.com for assistance.
Lighthouse Lab Services | 844-974-1929 | https://www.lighthouselabservices.com/

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