Clinical Research Executive

Company Description

IntelliMed Healthcare Solutions specializes in Contract/Outsourced Medical Affairs Services, ensuring that your product has the scientific edge needed to connect with and persuade stakeholders. With over 25 years of experience in medical affairs, our team is capable of managing scientific and medical support from conceptualization to delivery. We provide medical, clinical, and economic data, communication, and regulatory support. We partner with clients to build market access for pharmaceuticals, medical devices, and nutraceuticals, offering expertise in data generation, differentiation, and dissemination.

Role Description

This is a full-time, on-site role for a Clinical Research Executive located in the Mumbai Metropolitan Region. The Clinical Research Executive will be responsible for conducting market research, analyzing data, designing questionnaires, preparing presentations, and communicating effectively with stakeholders. The role requires performing detailed analysis and generating reports to support the business growth of our clients.

We are seeking a proactive and detail-oriented Clinical Research Executive to join our team at Intellimed Healthcare Solutions. The successful candidate will have 2-3 years of experience in clinical research, specializing in protocol development, CRF design, and study documentation. You will play a critical role in monitoring clinical trials and ensuring compliance with regulatory standards.

Key Responsibilities:

• Collaborate in developing and reviewing clinical trial protocols aligned with project requirements.
• Design, develop, and finalize Case Report Forms (CRFs) to ensure efficient data collection.
• Monitor clinical trial sites for regulatory compliance, data integrity, and protocol adherence.
• Maintain accurate and complete study documentation in line with Good Clinical Practice (GCP) standards.
• Coordinate with investigators and site staff for smooth trial execution.
• Conduct site visits and provide training/support to site personnel.
• Prepare monitoring reports, progress reports, and documentation for audits and regulatory submissions.
• Contribute to the overall quality, compliance, and timeliness of clinical research projects.

Qualifications:

• Science graduate with a qualification in clinical research
• 2-3 years of experience in clinical research, clinical trial management, or related fields.
• Knowledge of ICH-GCP guidelines, regulatory frameworks, and clinical trial procedures.
• Strong documentation, communication, and organizational skills.
• Ability to work onsite in Mumbai and adapt to a fast-paced environment.