Company Overview

Sir H. N. Reliance Foundation Hospital & Research Centre is a 345-bed, multi-specialty tertiary care hospital located in Mumbai, Maharashtra. Known for its technologically-advanced infrastructure, it operates to international standards offering cutting-edge services in various medical fields. The hospital is synonymous with excellence and respect for life, continuing its legacy of providing superior care and service. Visit our website at rfhospital.org.

Job Overview

We are seeking a qualified Senior Clinical Associate to join our esteemed team in Mumbai Suburban, Mumbai, Navi Mumbai. As a full-time role, the position requires expertise in clinical practices and procedures pertinent to our advanced and diverse healthcare services. This role involves coordination with various departments to ensure top-notch clinical services aligned with our commitment to excellence and care.

Qualifications and Skills

• Proficiency in Good Clinical Practice (Mandatory skill) to maintain the highest standards in clinical care and research methodologies.
• Extensive knowledge of Medical Terminology (Mandatory skill) pertinent to multi-specialty healthcare to ensure effective communication and understanding.
• Experience in Clinical Research Coordination (Mandatory skill), ensuring that all clinical trials are executed efficiently and ethically.
• Ability to proficiently use Clinical Trial Management Software for managing and monitoring clinical trials from inception to completion.
• Experienced in using Electronic Data Capture Systems for efficient handling and storage of clinical data that ensures accuracy and reliability.
• Strong understanding of Regulatory Compliance to ensure all clinical procedures adhere to set laws and institutional regulations.
• Competent in Data Analysis and Interpretation, allowing for effective decision-making based on interpreting complex datasets.
• Solid Project Management skills to lead and manage projects efficiently, ensuring objectives are met timely and within budget.

Roles and Responsibilities

• Oversee and coordinate clinical trials, ensuring adherence to stringent regulatory and ethical standards.
• Collaborate with cross-functional teams to facilitate smooth communication and operations in clinical research activities.
• Maintain accurate documentation of clinical protocols, records, and processes to ensure data integrity and compliance.
• Develop and implement strategies for effective participant recruitment and retention throughout clinical trials.
• Interpret and analyze clinical data to generate reports that aid in strategic decision-making for the organization.
• Provide training and guidance to junior staff and clinical research teams to ensure high standards of performance.
• Liaise with external stakeholders such as regulatory bodies and research institutions to foster collaborative partnerships.
• Respond promptly to any issues or challenges that arise during clinical trials, ensuring minimal disruption to operations.