Contract Clinical Research Associate

Actalent; San Diego (CA); À distance; USD 96 000 - 131 000; Plein temps

Résumé du poste

Actalent seeks a Clinical Research Associate (CRA) for a 6-month renewable contract (to hire) based in San Diego, CA. The role is 100% remote with 60-80% travel. Any therapeutic background is acceptable.

You will monitor investigator sites, ensure protocol and regulatory compliance, manage essential documents, and support data integrity. The position requires 2+ years of CRA experience and a life sciences degree or RN qualification.

Qualifications

• Bachelor's degree in life sciences or RN required.
• Minimum 2+ years of clinical research monitor experience.
• Valid driver's license where applicable.
• Strong ICH-GCP knowledge and regulatory understanding.
• Excellent verbal and written English communication.

Responsabilités

• Monitor investigator sites using risk-based monitoring and address issues.
• Verify data accuracy via source data review and CRF checks.
• Assess investigational products through inventory and records review.
• Escalate deficiencies to clinical management and ensure resolution.
• Maintain regular contact with sites to ensure protocol adherence.
• Perform monitoring per the monitoring plan and assist investigator payments.
• Provide trial status updates to the Clinical Team Manager.
• Keep study systems updated and perform quality checks in CTMS.
• Participate in investigator meetings and identify qualified sites.
• Initiate sites per procedures to ensure regulatory compliance.
• Ensure essential documents are complete per ICH-GCP.
• Support project publications/tools with ideas and input.
• Facilitate communication between sites, client, and project team.
• Respond to regulatory requests, audits, and inspections.
• Complete administrative tasks like expense reports and timesheets.
• Contribute to process improvement initiatives.

Connaissances

Bachelor's degree life sciences / RN

2+ years CRA experience

Valid driver's license

ICH-GCP knowledge

Critical thinking

Risk based monitoring

Oral & written communication

Detail-oriented

Team work / independence

MS Office / software aptitude

English grammar

Formation

Bachelor's degree life sciences or RN

Outils

MS Office

Description du poste

w2 or 1099 contract

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.

#ActTFjobs26

Job Type & Location

This is a Contract position based out of San Diego, CA.

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)

Job Type & Location

This is a Contract position based out of San Diego, CA.

Application Deadline

This position is anticipated to close on Oct 27, 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.