Credevo Hiring For Quality Assurance Associate

Credevo is hiring for the position of Quality Assurance Associate on a remote basis. The role requires 4+ years of experience and an immediate joiner. The position focuses on quality assurance, GCP compliance, clinical trial data integrity, documentation, audits, and process improvement.

Job Details

Position

Quality Assurance Associate

The Quality Assurance Associate will support QA processes in clinical research, ensuring compliance with Good Clinical Practice (GCP), SOPs, regulatory requirements, and company policies. The role also involves clinical trial data review, audits, documentation, risk management, and process improvement.

Key Responsibilities

Data Integrity and Accuracy

• Review and verify clinical trial data for accuracy, completeness, and consistency.
• Ensure clinical trial data is generated, recorded, and reported according to protocols, SOPs, and GCP.
• Participate in data validation and reconciliation activities.

Compliance and Regulatory Adherence

• Maintain knowledge of GCP guidelines, regulatory requirements, and company policies.
• Ensure clinical trial activities comply with relevant regulations and guidelines.
• Assist with preparation for and participation in audits and inspections.

Documentation and Record Keeping

• Maintain accurate and complete documentation of QA activities.
• Ensure proper storage and retrieval of clinical trial documents.
• Assist in developing and maintaining SOPs.

Process Improvement

• Identify areas for improvement in clinical trial processes and procedures.
• Contribute to the development and implementation of quality assurance plans.

Collaboration and Communication

• Collaborate with clinical research associates, data managers, and regulatory affairs staff.
• Communicate findings and recommendations to management and stakeholders.

Eligibility and Qualifications

Candidates should have:

• 4+ years of experience
• A Bachelor’s degree in a related field, such as:
  • Life Sciences
  • Pharmacy
  • Nursing
• Familiarity with GCP guidelines and regulatory requirements
• Knowledge of clinical trial data management systems and electronic data capture (EDC) systems
• Understanding of clinical trial processes and procedures

Required Skills

• Strong attention to detail and accuracy
• Excellent organizational and communication skills
• Ability to work independently and as part of a team
• Proficiency in data analysis and interpretation

Application Details

Interested candidates can apply for the Quality Assurance Associate position through the application form provided below.