Expert in Clinical Study Documentation and Regulatory Compliance

Job Title: Clinical Documentation SpecialistJob Summary:This role involves reviewing patient medical records to ensure accurate coding and compliance with regulatory requirements.Main Responsibilities:Assign accurate codes to patient medical recordsEnsure adherence to coding guidelines and regulatory requirementsCollaborate with healthcare professionals to...

Regulatory Compliance ExpertAbout the Role:We seek a highly skilled Regulatory Compliance Expert to ensure adherence to regulatory requirements and implement effective quality management systems.Main Responsibilities:Document Control: Prepare and review QMS-related documents, including SOPs, work instructions, and templates for validation, qualification, and...

Regulatory Affairs SpecialistWe are seeking a highly skilled Regulatory Affairs professional with expertise in both pharmaceutical and medical device regulatory compliance.The role involves preparing, reviewing, and submitting regulatory documentation to global health authorities, ensuring compliance with applicable regulations.Main...

Job Title: Clinical Research Operations Manager.Job Summary As a clinical research operations manager, you will be responsible for overseeing the day-to-day operations of clinical trials. This includes collaborating with project managers to set targets for clinical monitoring staff, ensuring compliance with project goals. You will also create and implement...

Clinical Research Associate Job OverviewWe are seeking a skilled Clinical Research Associate to join our team.Job Description:The successful candidate will be responsible for authoring and analyzing clinical trial documents, working with key clinical documents such as protocols, informed consent forms, and clinical study reports. They will also create,...

Job OpportunityWe seek a skilled Regulatory Chemist to perform critical tasks in product regulatory approval.Purpose and ResponsibilitiesPrepare and submit regulatory documents for compliance review.Develop strategies to meet evolving regulatory demands.Coordinate product registration with provincial guidelines and third-party suppliers.RequirementsTo...

Job DescriptionThe Senior Claims Processing Specialist oversees all aspects of charge creation and capture, ensuring accurate and compliant billing practices. This role acts as liaison for clinical areas and revenue cycle on proper documentation, coding, and billing procedures.This specialist plays a critical role in maximizing revenue integrity, minimizing...

As a senior medical professional, you will lead our team in clinical and post-marketing drug safety initiatives.Clinical Phase:Act as a medical monitor/medical expert, ensuring effective communication with clients and support to sites regarding protocol or possible drug interactions.Review and provide feedback on study protocols as needed, delivering...

At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.We are looking for a Senior Clinical Data Manager I to join our A-team.The Senior Clinical Data Manager I (SrCDM1) is responsible for leading data...

JOB DETAILS 1.Collaborating with Project Manager to set targets for clinical monitoring staff, and ensuring recording of trial in compliance with project goals.2.Creating and implementing study-specific clinical monitoring tools and documents.3.Creating and overseeing trial budget.4.Identifying, enlisting and choosing sites, and coordinating site management...