Clinical Research Analyst

Location

Ludhiana | India

Job description

AccuScript Consultancy is looking for Clinical Research Analyst to join our dynamic team and embark on a rewarding career journey

• A Clinical Research Analyst plays a crucial role in the planning, implementation, and analysis of clinical research studies
• The primary responsibilities include collecting, organizing, and interpreting clinical data to support the development and improvement of medical treatments and interventions
• The Clinical Research Analyst collaborates with cross-functional teams, ensures adherence to regulatory requirements, and contributes to the overall success of clinical research projects

Key Responsibilities:

• Study Planning and Design:Participate in the development of research protocols and study designs
• Contribute to the planning and execution of clinical trials, ensuring compliance with ethical and regulatory guidelines
• Data Collection and Management:Oversee the collection, validation, and maintenance of clinical data
• Implement data quality control procedures to ensure accuracy and completeness
• Manage electronic data capture systems and databases
• Statistical Analysis:Perform statistical analysis of clinical trial data using appropriate software
• Generate and interpret statistical reports to support decision-making and regulatory submissions
• Collaborate with biostatisticians to ensure proper study design and statistical methodologies
• Regulatory Compliance:Stay abreast of regulatory requirements and guidelines applicable to clinical research
• Ensure study protocols, informed consent forms, and other essential documents comply with regulatory standards
• Collaboration and Communication:Collaborate with cross-functional teams, including investigators, clinical coordinators, and regulatory affairs
• Communicate effectively with internal and external stakeholders, presenting findings and updates
• Quality Assurance:Implement quality assurance processes to ensure data integrity and regulatory compliance
• Contribute to the development and improvement of Standard Operating Procedures (SOPs) related to clinical research
• Project Management:Assist in the coordination and management of clinical research projects
• Monitor timelines, milestones, and deliverables to ensure the successful completion of studies

Job tags

Salary