Clinical Research Associate (CRA)
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| Company Name | Planet Pharma |
| Company Type | Private |
| Job Type | Contract |
| Salary Range | Market Competitive |
| Location | Carlsbad, CA |
| Qualifications | None / No Formal Education |
| Experience | No Experience / Fresh |
Job Overview
Planet Pharma is seeking a Clinical Research Associate (CRA) to join their team in Carlsbad, CA. This contract role involves contributing to crucial life sciences research, focusing on pharmaceuticals, biotechnology, or medical devices, and ensuring the integrity and compliance of clinical trials.
Company Overview
Founded in 2012, Planet Pharma is a global leader in life sciences recruitment and staffing. They specialize in Pharmaceuticals, Biotechnology, Medical Device, Labs & Healthcare, Specialty Providers, CMOs / CDMOs, and Contract Research Organizations (CROs). With offices across North America, Europe, and APAC, Planet Pharma offers comprehensive staffing solutions including Contract & Direct Hire, Strategic Resourcing, Retained & Executive Search, Functional Service Provider (FSP), and Global Workforce Solutions, operating with shared attributes at the heart of everything they do.
Quick Details
- Salary Range: Market Competitive
- Job Type: Contract
- Qualifications: None / Open to all applicants
- Experience: No Experience / Fresh
Key Responsibilities
- Conduct on-site and remote monitoring visits to ensure trial adherence to protocol, GCP, and regulatory requirements.
- Verify source data, ensure accurate data entry, and resolve data queries effectively.
- Manage trial essential documents and maintain the Trial Master File (TMF) for assigned studies.
- Communicate effectively with site staff, investigators, and study team members.
- Participate in investigator meetings and provide site staff training as needed.
- Assist with site selection, initiation, and close-out activities.
Requirements
- Strong understanding of ICH-GCP guidelines and applicable regulatory requirements.
- Excellent communication, organizational, and interpersonal skills.
- Ability to work independently, prioritize tasks, and manage multiple projects efficiently.
- Proficiency in using clinical trial management systems and other relevant software.
- Willingness and ability to travel for site visits as required.
- Detail-oriented with a commitment to quality and accuracy in all aspects of work.
Benefits
- Opportunity to work with a global leader in life sciences recruitment and staffing.
- Exposure to diverse and impactful projects within pharmaceuticals, biotechnology, and medical devices.
- Professional development and career growth opportunities within a dynamic industry.
- Collaborative and supportive team environment across multiple global offices.
- Competitive contract compensation for your contributions.
- Access to a broad network of professionals and opportunities within the life sciences industry.