Senior Clinical Document Specialist

Job Title: Clinical Documentation Specialist We are seeking a detail-oriented and analytical Clinical Documentation Specialist to join our team. The successful candidate will be responsible for analyzing and translating clinical records into standard medical codes. Key Responsibilities:Accurately translate clinical records into standard medical codesReview...

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,...

Job Title: Clinical Quality Assurance Compliance & trainingExperience: 5 plus yearsLocation: MumbaiType: Full-timeExperience Level: [Senior] Manager/Senior ManagerDepartment: Clinical Research Department Purpose of this Role:This role will be responsible for oversight on end-to-end clinical trial activities from quality perspective. This role will be...

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">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:">

Job Title:">Sr Medical Writer - Clinical Document Specialist">">Lead the development and execution of clinical document strategies for trial projects.">Collaborate with cross-functional teams to interpret and analyze data, summarize scientific findings, and communicate insights in written form.">Participate in planning and execution of clinical development...

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.

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,...