Clinical Project Associate

Clinical Project Associate
  • Competitive
  • Temporary
  • Foster City CA, US Foster City SAN MATEO US 94404
Job Ref: JO000115116
Sector: Clinical
Sub-sector: Clinical
Date Added: 21 April 2021

Clinical Project Associate

Development: Primarily responsible for the business, operational, and compliance aspects of drug discovery, development, and marketed products.

Job Family

Clinical Operations: Clinical Operations is responsible for the execution of all Phase 1-4 clinical trials, across all therapeutic areas, around the world. In partnership with Clinical Research, Medical Affairs and Development Operations functions, ensures that all clinical trial activities are performed in accordance with all applicable SOPs, company policies and regulatory guidelines to provide timely delivery of high-quality clinical data to support global registration and commercialization of products.

Project Involvement

• Project involvement will be in a supportive role

Key Differentiating Contributions

• Ability to take direction from senior team members

• Collaborative demeanor

• Great organizational skills

• Strong computer technical skills (word processing and spreadsheet development)

Job Responsibilities and Skills

• Excellent verbal and written communication skills

• Must be able to work both independently and as part of a team

• Tracks and prepares study-specific information utilizing databases, spreadsheets and other tools

• Reviews and participates in the quality assurance of data or documents

• Arranges meeting logistics, agendas, and assists with minutes

• Serves as back up providing verbal and written communication with study personnel

• Assists with development of documents and standard forms

• Provide input and assist with harmonization of Clinical Operations databases and tracking tools

• Assist in maintaining clinical information and training of Clinical Operations personnel in the clinical trials management system (GILDA)

• Serves as CTMA back up providing verbal and written communication with study personnel

• Interacts with other departments, as directed, to complete assigned tasks

• May assist with monitoring visits under the direct supervision of senior staff

• Assists with the planning and facilitation of investigator meetings and, when applicable, provides onsite support during the meetings

• Knowledge of FDA and EMA Regulations, ICH Guidelines, GCP, and familiarity with standard clinical operating procedures

• Must be familiar with Word, PowerPoint, and Excel

• Travel may be required

Minimum Education and Experience

• At least 1+ year of experience and a BS or BA in a relevant scientific discipline

• At least 1+ year of experience and an RN (2 or 3-year certificate)


SRG is an Equal Opportunity Employer - All qualified applicants will receive consideration without regard to race, color, religion, gender, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law.

21/05/2021 12:00:00
USD 0.00 0.00 Hour
Contact Consultant:
Brian Houston

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