Shree Clinical Services Pvt Ltd A clinical research organization specializing in managing and conducting clinical trials across multiple therapeutic areas such as oncology, cardiovascular diseases, and vaccines. The company ensures compliance with Good Clinical Practice (GCP) guidelines and provides end-to-end clinical trial management, including patient recruitment, regulatory documentation, and data analysis Show more Show less
Company Description Shree Clinical Research excels in conducting multi-centre, multi-geography clinical trials, with a strong focus on establishing long-term partnerships with Sponsors, investigators, sites, and patients. We provide tailored end-to-end solutions for any aspect of clinical research. Equipped with ICH GCP, Standard Operating Procedures (SOPs), all our clinical trial activities strictly comply with regulatory principles and guidelines. We adhere to the highest standards of ethics to ensure patient safety and confidentiality. Role Description This is a full-time on-site role for a Sr. Clinical Research Coordinator located in Belgaum. The Sr. Clinical Research Coordinator will be responsible for overseeing clinical trials, obtaining informed consent, managing protocols, and ensuring compliance with regulatory guidelines. The role involves coordinating with investigators, sites, and patients, and ensuring the smooth execution of clinical research activities. Qualifications Experience in Clinical Research and Clinical Trials Proficiency in handling Informed Consent Knowledge of Protocol and Research methodologies Strong organizational and communication skills Ability to work independently and collaboratively Bachelor's degree in a relevant field, such as Life Sciences, or equivalent experience Familiarity with ICH GCP and SOPs is a plus
The Sr. Clinical Research Coordinator position at Shree Clinical Research in Belgaum is a full-time on-site role that involves overseeing clinical trials, managing protocols, and ensuring regulatory compliance. In this role, you will be responsible for obtaining informed consent, coordinating with investigators, sites, and patients, and ensuring the smooth execution of clinical research activities. To qualify for this position, you should have experience in Clinical Research and Clinical Trials, proficiency in handling Informed Consent, knowledge of Protocol and Research methodologies, strong organizational and communication skills, and the ability to work both independently and collaboratively. A Bachelor's degree in a relevant field like Life Sciences or equivalent experience is required. Familiarity with ICH GCP and SOPs is considered a plus. Shree Clinical Research focuses on conducting multi-centre, multi-geography clinical trials and aims to establish long-term partnerships with Sponsors, investigators, sites, and patients. Equipped with ICH GCP and SOPs, the company ensures that all clinical trial activities adhere to regulatory principles and guidelines, maintaining the highest standards of ethics to safeguard patient safety and confidentiality.,
As a clinical research organization, Shree Clinical Services Pvt Ltd specializes in managing and conducting clinical trials across various therapeutic areas including oncology, cardiovascular diseases, and vaccines. The company is dedicated to ensuring compliance with Good Clinical Practice (GCP) guidelines to maintain high standards in the industry. Shree Clinical Services Pvt Ltd offers end-to-end clinical trial management services which include patient recruitment, regulatory documentation, and thorough data analysis. By leveraging their expertise and experience, the company aims to contribute significantly to the advancement of medical research and healthcare.,
Role Overview: As a member of Shree Clinical Services Pvt Ltd, you will be part of a clinical research organization that specializes in managing and conducting clinical trials across various therapeutic areas like oncology, cardiovascular diseases, and vaccines. The company places a strong emphasis on ensuring compliance with Good Clinical Practice (GCP) guidelines. Your role will involve providing end-to-end clinical trial management, which includes tasks such as patient recruitment, regulatory documentation, and data analysis. Key Responsibilities: - Manage and conduct clinical trials in oncology, cardiovascular diseases, vaccines, and other therapeutic areas - Ensure compliance with Good Clinical Practice (GCP) guidelines throughout all trial activities - Oversee patient recruitment efforts for clinical trials - Handle regulatory documentation required for conducting clinical trials - Analyze and interpret data collected during clinical trials Qualifications Required: - Bachelor's degree in a relevant field such as life sciences, pharmacy, or healthcare - Prior experience in clinical trial management is preferred - Strong understanding of Good Clinical Practice (GCP) guidelines and regulatory requirements - Excellent communication and organizational skills - Ability to work effectively in a team environment (Note: No additional details about the company were provided in the job description.),