Clinical Documentation Specialist

Greetings from Star SecutechHuge openings for Immediate JoinersRole: Clinical Documentation Reviewer (International Helathcare)Minimum 2 years of experience in International HealthcareWork experience as Clinical documentation specialist, claim officer (on paper)Work From Office positionWe are looking for immediate joinersExcellent communication skills are...

Key Clinical Trial Documents SpecialistDevelops high-quality clinical trial documents, including protocols, Investigator's Brochures (IBs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), and Clinical Study Reports (CSRs).Translates complex scientific data into clear, regulatory compliant documents supporting drug development and approval...

Clinical Research Associate RoleWe are seeking a skilled Clinical Research Associate to conduct clinical trial authoring and analysis tasks. As a key member of our team, you will be responsible for producing high-quality clinical documents.Key Responsibilities:Author and analyze clinical trial documents.Work with key clinical documents including protocol,...

Clinical Publishing Coordinator Job SummaryWe are seeking a highly skilled Clinical Publishing Coordinator to join our team. The successful candidate will be responsible for creating and modifying clinical investigator manuals, requisitions and other relevant materials according to SOW requirements.Key Responsibilities:Create and modify clinical investigator...

Job Summary:We are seeking a highly skilled and detail-oriented Medical Document Reviewer to join our team. As a key member of our medical review process, you will be responsible for reviewing and assessing medical documents, including clinical trial data, safety reports, and regulatory submissions.

Job Title: Clinical Research Associate (CRA)Company: MS Clinical Research Pvt LtdAbout Us:MS Clinical Research (MSCR) is a leading clinical research organization dedicated to advancing scientific discovery and improving healthcare outcomes. We are committed to conducting high-quality clinical trials and contributing to the development of innovative medical...

Company DescriptionCalibration Center A Unit Of Nagman Instruments Electronics Private Limited is an electrical/electronic manufacturing company based in Chennai, Tamil Nadu, India. We specialize in solutions for precision measurement and calibration. Our advanced manufacturing practices and state-of-the-art facilities ensure that we meet the highest...

Job Summary">As a Medical Document Reviewer, you will play a vital role in ensuring the accuracy and integrity of medical documents. This includes clinical trial data, safety reports, and regulatory submissions.Key Responsibilities:">

Your Role:As a Senior Associate/Specialist Document Coordinator, you will support the Global Medical Writing Team to deliver its portfolio effectively and efficiently. This role involves managing the quality review of clinical and regulatory documents Conducting quality review of clinical and regulatory documents, including Protocols, Clinical Study Reports,...

Medical Writer/Clinical Study ResearcherWe are seeking a Medical Writer/Clinical Study Researcher to join our team. As a key member of our clinical research team, you will play a crucial role in developing high-quality clinical trial documents.