Clinical Trial Assistant

Company DescriptionHREE Research Pvt. Ltd. is a full-service Clinical Research Organization (CRO) offering comprehensive, end-to-end clinical research solutions. We specialize in supporting pharmaceutical, biotechnology, and medical device companies across all phases of clinical trials. Our services include study design and protocol development, regulatory...

Job Title: AGM / DGM – Clinical Trials (Protocol & Report Writing)Department: Clinical Research / Clinical OperationsMinimum 10–15 yrs of relevant experience in clinical trials, protocol writing, CSR writing, and regulatory documentation

The Clinical Trial Physician is responsible for providing medical input within the organization as well as to external partners and performing medical review tasks within the context of clinical trials. Furthermore, the Clinical Trial Physician is responsible for undertaking scientific/medical writing tasks within the organization.Role & responsibilitiesIs...

The Clinical Trial Physician is responsible for providing medical input within the organization as well as to external partners and performing medical review tasks within the context of clinical trials. Furthermore, the Clinical Trial Physician is responsible for undertaking scientific/medical writing tasks within the organization. Role & responsibilities Is...

Clinical Trial Coordinator - Mumbai for Pharma Company **Qualification**: - A post-graduate in life sciences/PharmD - GCP trained and Certified **Required Skills**: - Thorough understanding of drug development process and expertise in NDCT rules & ICH-GCP/Indian GCP - Knowledge of clinical trial regulation of US FDA, EMEA, NDCT rules, ICMR guidelines. -...

Advanced Clinical is a clinical development and strategic resourcing organization committed to providing a better clinical experience across the drug development journey. Our goal is to improve the lives of all those touched by clinical research – approaching each opportunity with foresight, character, resilience and innovation. Based on decades of...

Role & responsibilitiesResponsible for clinical trial medical science related activities like preparation of protocol, Informed consent form, CRF, other study related documents and SOPs in line with ICH GCP, Indian and global regulatory.Conduct relevant literature search for required for protocol and manuscript writing.Ensures that medical writing...

Job Type- Fresher or Internship levelClinical Research Associates manage clinical trials and studies pertaining to biotechnological and pharmaceutical products, drugs and procedures. A Clinical Research Associate, also known as a CRA, conducts research to ensure these products are safe.Responsibilities:Assist in Protocol Development:Collaborate with the...

**Job Summary**: We are seeking a highly motivated and organized Clinical Research Coordinator (CRC) to manage and coordinate clinical trials, ensuring compliance with regulatory guidelines and protocols. The CRC will work closely with principal investigators, study participants, and regulatory bodies to support successful trial execution. **Key...

Coordinate day-to-day activities of clinical trials from initiation to close-out. Recruit, screen, and enroll eligible participants as per study protocol. Schedule and conduct study visits, ensuring adherence to study timelines. Maintain accurate and timely documentation including case report forms (CRFs), informed consent forms (ICFs), and other...