Contract Senior CRA

Actalent; Nashville (TN); À distance; USD 96 000 - 131 000; Temps partiel

Avantages offerts par ce poste

Medical, dental & vision

401(k) retirement plan

PTO / Time Off

Life Insurance

Résumé du poste

Actalent is seeking a Clinical Research Associate (CRA) for a 6‑month renewable contract based out of Nashville, TN. The role supports remote and on‑site monitoring to ensure protocol adherence, regulatory compliance, and data integrity across sites.

Travel will be 60%–80%, with an emphasis on risk‑based monitoring and audit readiness. The ideal candidate holds a life sciences degree or RN, has 2+ years of CRA experience, and demonstrates strong ICH‑GCP knowledge and communication skills.

Qualifications

• Bachelor's degree in life sciences or RN.
• Minimum of 2+ years of experience as a clinical research monitor.
• Valid driver's license where applicable.
• Strong understanding of ICH‑GCPs and applicable regulations.
• Excellent written and verbal communication and documentation skills.

Responsabilités

• Monitor investigator sites using risk‑based monitoring and perform root cause analysis to address site issues.
• Ensure data accuracy via source data verification and CRF review during on‑site and remote visits.
• Assess investigational products through inventory checks and records review with compliant reporting.
• Escalate deficiencies to clinical management and drive timely resolution.
• Maintain regular contact with sites to confirm protocol adherence and issue resolution.
• Complete administrative tasks including expense reports and timesheets promptly and support project publications/tools.

Connaissances

Life sciences degree

CRA experience

ICH-GCP knowledge

Documentation

Travel readiness

Strong communication

Formation

Bachelor's degree in life sciences or RN

Description du poste

w2 or 1099 contract - DOOR TO DOOR PAY

6 month renewable or contract to hire (convert to perm)

Any therapeutic background is OK

Large CRO!

Job Title: Clinical Research Associate (CRA)

Job Description

This position involves performing and coordinating all aspects of the clinical monitoring and site management process. The role requires conducting remote or on‑site visits to assess protocol and regulatory compliance, managing required documentation, and ensuring that trials are conducted in accordance with approved protocols, ICH‑GCP guidelines, and applicable regulations. The CRA will act as a site processes specialist, ensuring the rights and well‑being of subjects and the reliability of data. The position also involves developing collaborative relationships with investigational sites and ensuring audit readiness.

Responsibilities

• Monitor investigator sites using a risk‑based monitoring approach, applying root cause analysis, critical thinking, and problem‑solving skills to identify and rectify site process failures.
• Ensure data accuracy through source data review, source document verification, and case report form review during on‑site and remote monitoring activities.
• Assess investigational products through physical inventory and records review, documenting observations in reports and letters using approved business writing standards.
• Escalate observed deficiencies and issues to clinical management and ensure their resolution.
• Maintain regular contact with investigative sites to confirm protocol adherence and timely issue resolution.
• Conduct monitoring tasks in accordance with the approved monitoring plan and participate in the investigator payment process.
• Provide trial status tracking and progress update reports to the Clinical Team Manager.
• Ensure study systems are updated per agreed study conventions and perform quality control checks of reports generated from the Clinical Trial Management System.
• Participate in investigator meetings and identify potential investigators to ensure qualified investigative sites.
• Initiate clinical trial sites according to relevant procedures to ensure compliance with protocols and regulatory obligations.
• Ensure that required essential documents are complete and in place according to ICH‑GCP and applicable regulations.
• Contribute to project team efforts by assisting in the preparation of project publications/tools and sharing ideas/suggestions.
• Facilitate effective communication between investigative sites, the client company, and the project team.
• Respond to company, client, and applicable regulatory requirements, audits, and inspections.
• Complete administrative tasks such as expense reports and timesheets promptly.
• Contribute to other project work and initiatives for process improvement as required.

Essential Skills

• Bachelor's degree in a life sciences‑related field or a Registered Nursing certification or equivalent formal academic qualification.
• Minimum of 2+ years of experience as a clinical research monitor.
• Valid driver's license where applicable.
• Effective clinical monitoring skills.
• Understanding of medical/therapeutic area knowledge and medical terminology.
• Strong grasp and application of ICH‑GCPs, applicable regulations, and procedural documents.
• Well‑developed critical thinking skills for in-depth investigation and root cause analysis.
• Ability to manage Risk Based Monitoring concepts and processes.
• Effective oral and written communication skills with medical personnel.
• Strong customer focus and attention to detail.
• Effective interpersonal skills and strong attention to detail.
• Good organizational and time management skills.
• Ability to work independently or within a team as required.
• Proficient computer skills, including knowledge of Microsoft Office and the ability to learn appropriate software.
• Good English language and grammar skills.

Additional Skills & Qualifications

• Experience in remote or on‑site visits to assess protocol and regulatory compliance.
• Experience managing procedures and guidelines from different sponsors and monitoring environments.
• Experience developing collaborative relationships with investigational sites.
• Experience ensuring audit readiness.

Work Environment

This position is 100% home-based with 60‑80% travel required.

Job Type & Location

This is a Contract position based out of Nashville, TN.

Pay And Benefits

The pay range for this position is $70.00 - $95.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job‑related factors.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan
• Pre‑tax and Roth post‑tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long‑term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

Application Deadline

This position is anticipated to close on Nov 12, 2026.

Workplace Type

This is a fully remote position.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News‑Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [e-mail] for other accommodation options.

San Francisco Fair Chance Ordinance

Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI)

We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.