Clinical Document Management Specialist

Job RoleKey Responsibilities:Publish clinical documents in accordance with organizational standards and KPIs.Perform quality control of published documents to ensure electronic functionality and adherence to internal and external document standards.Develop and maintain knowledge of current electronic publishing standards, regulatory guidelines, and legal...

Job OverviewWe are seeking a skilled Regulatory Writer to join our team. The successful candidate will be responsible for authoring and reviewing high-quality clinical and safety documents, including non-registration Clinical Study Reports (CSR), Development Safety Update Reports (DSUR), and Risk Management Plans (RMP).As a key member of the Clinical Trial...

Job Title: Clinical Documentation ManagerJob DescriptionWe are seeking a skilled and experienced Clinical Documentation Manager to join our team. In this role, you will be responsible for managing clinical documentation for various projects, including in-licensing, out-licensing, acquisitions, and divestments.Key Responsibilities:Act as the point of contact...

Job Description">">Drive the planning and execution of migrations to and from electronic document management systems (eDMS) in line with business, compliance, and operational requirements.">Collaborate with stakeholders to identify and agree on migration business requirements, understand source and target system capabilities, and develop a future migration...

Clinical Documentation Specialist Role:We are seeking a skilled Clinical Documentation Specialist to join our team. In this critical role, you will review clinical documentation in electronic health records to ensure accuracy, completeness, and compliance with coding standards.Key Responsibilities Include:Conduct concurrent reviews of inpatient records using...

Medical Writer Role">This is a Medical Writer role in the development and review of clinical and regulatory documents. The responsibilities include writing and reviewing various documents, ensuring adherence to established guidelines and regulations.ResponsibilitiesWrite and review clinical/regulatory documents such as clinical trial protocols, clinical...

Job Title: Document Management Specialist">Process clinical study documents in accordance with client and project requirements, adhering to SOPs/WPs and relevant regulations.Liaise with project teams and other staff to ensure effective fulfillment of responsibilities.Complete assigned projects within specified timelines, ensuring adherence to regulatory...

About this roleThis position involves leading and collaborating with cross-functional teams to ensure seamless transitions of documentation related to business development and licensing projects.The ideal candidate will have strong organizational awareness, excellent influencing and presentation skills, and the ability to communicate effectively at all...

Job Description:We are seeking a skilled Medical Writer to join our team. As a Medical Writer, you will be responsible for creating high-quality clinical and safety documents that meet regulatory requirements.You will author and review CSR, DSUR, RMP documents.You will lead outsourced Narrative projects and coordinate other outsourced activities in RWS.You...

Thryve Digital Health LLP is an emerging global healthcare partner that delivers strategic innovation, expertise, and flexibility to its healthcare partners. Being a US healthcare conglomerate captive, we have direct access to deeper insights that help us accelerate our learning process and keeps us ahead of the curve. Thryve delivers next-generation...