Clinical Documentation Specialist

Job Title: Clinical Research Documentation SpecialistAbout the Role:We are seeking an experienced Clinical Research Documentation Specialist to join our team. As a key member of our clinical operations group, you will play a critical role in developing high-quality clinical trial documents.Key Responsibilities:Developing Key Clinical Trial...

Clinical Research AssociateAbout Us:We are a global company that partners with major firms in healthcare, telecom, and media. Our team combines deep industry expertise with agile development practices to enable scalable and cost-effective digital transformation.The position is for a Clinical Document Authoring Specialist who will work on clinical trial...

Clinical Research Associate">Job Summary: We are seeking a highly motivated Clinical Research Associate to play a key role in the clinical trials process.Clinical Research Associates work closely with investigators and research teams to ensure compliance with regulations and guidelines. Their primary responsibilities include coordinating on-site trial...

Clinical Quality Assurance SupportWe are seeking a highly experienced Clinical Quality Assurance Specialist to provide day-to-day support across ongoing clinical trials. This individual will play a key role in guiding study teams, maintaining compliance with Good Clinical Practice (GCP), and ensuring quality oversight.Key ResponsibilitiesProvide QA expertise...

We are seeking a highly skilled medical professional to manage medical records and documentation.The ideal candidate will have experience in medical record-keeping, transcription, and coding. They will be responsible for reviewing physician dictation, transcribing clinical notes into electronic health records (EHRs) and preparing medical record...

Job OpportunityWe are seeking a highly skilled Clinical Monitoring Expert to play a pivotal role in ensuring the quality and integrity of clinical trial data through centralized monitoring activities, statistical data review, and proactive risk management.The ideal candidate will possess a strong understanding of ICH GCP guidelines and the clinical...

Job Title: Clinical Data ProgrammerWe are seeking a highly skilled Clinical Data Programmer to join our team. The ideal candidate will have hands-on experience with reviewing clinical data in JReview and collaborating with internal/external stakeholders and data engineers.

Documentation Specialist RoleWe are seeking a skilled professional to join our organization as a Documentation Specialist. The ideal candidate will be responsible for creating high-quality technical documentation, including user manuals and guides.Main Responsibilities:Write and maintain User Manuals for model libraries and tools methodologies.Develop...

Clinical Cancer ExpertWe are seeking a highly skilled Clinical Cancer Expert to join our team. The ideal candidate will possess strong clinical skills and experience in surgical oncology.About the Role:Diagnose and treat various types of cancers using state-of-the-art techniques.Conduct thorough consultations with patients, providing personalized guidance...

Site Report SpecialistThe Site Report Specialist plays a critical role in ensuring the quality and integrity of site visit reports. They review SVRs to ensure compliance with IQVIA SOP, ICH/GCP guidelines, and protocol requirements.Key Responsibilities:Oversee a caseload of SVRs for assigned studies, ensuring compliance to the protocol, processes, timelines,...