Role Description To drive continued success in this exciting clinical research field, we are seeking a committed, skilled, and customer-focused individual to join our winning team as a Medical Writer for our Toronto/Markham, Ontario, Canada on-site location, or remotely from a home-based office anywhere in Canada in accordance with our Work from Home policy. - Work closely with the Everest project team members assigned to the project to achieve project milestones according to the project timeline. - Perform Everest internal QC procedures for clinical documents developed by other Medical Writers, such as: - Clinical study protocols - Clinical Study Reports (CSRs; full, abbreviated, or synoptic) - Pharmacokinetic (PK) reports - Statistical reports - Integrated efficacy or safety summaries - Patient narratives - Manuscripts, posters, and abstracts - Apply therapeutic area experience and scientific knowledge in the review and include QC checks for: - Protocol-related information - Accuracy of in-text numbers and source references - Consistency of document styles and formats - Act as a lead medical writer in the preparation of clinical documents or scientific publications. - Perform literature searches to support senior medical writers. - Perform document e-publishing for CSRs and other clinical/regulatory documents. - Plan and manage deliverables and timelines in accordance with clinical trial project teams’ requirements. - Keep current on the training of Everest Guidance Documents and with the general requirements or guidelines issued by the pharmaceutical drug trial regulators and ICH. - Plan and carry out professional development. Qualifications - Advanced degree, Ph.D. preferred, in Clinical or Medical or Life Sciences, or Master’s degree with substantial experience in the subject matter. - At least two years' experience in medical writing practice, with experience in the pharmaceutical clinical trial environment. - Experience with medical writing for clinical study reports for regulatory submission (preferred). - Experience in multiple therapeutic areas and Phase I through IV clinical trials an asset (preferred). - Excellent understanding of clinical trials and common clinical trial statistical analysis methods (preferred). - Demonstrated ability to understand medical information and results; able to communicate effectively, orally and in writing. - Ability to handle multiple projects and clients. - Excellent interpersonal and teamwork skills; detail-oriented, customer- and quality-focused. - Demonstrated experience, knowledge, and understanding of GCP/ICH guidelines, including E3 Structure and Content of Clinical Study Reports. - Well organized and able to work independently. - Comprehensive skills in Microsoft Office applications and Adobe Acrobat. Computing skills with TRS Toolbox pharma edition plugin an asset. Requirements - Strong foundation in statistical and data management. - Ability to perform effective editing on assigned medical writing products. - Experience in performing QC checks on medical writing deliverables. - Ability to incorporate reviewers’ comments/input into draft documents. - Experience in finalizing documents for delivery to Sponsors according to established timelines. Benefits - Robust benefits package including medical, dental, and vision coverage. - Life & AD&D insurance. - Short- and long-term disability. - Tuition reimbursement. - Fitness reimbursement. - Employee assistance program (EAP). - Pension plan. - Generous paid time off and sick leave. - Opportunity to earn a performance-based bonus.

• Review and evaluate medical record documentation for completeness, accuracy, and compliance. • Collaborate with physicians, nurses, and coding professionals to ensure appropriate clinical documentation. • Identify opportunities for documentation improvement to support coding accuracy, reimbursement, and clinical outcomes. • Analyze medical records to ensure documentation supports quality care and appropriate reimbursement. • Formulate compliant, clinically sound physician queries.

• Use clinical and coding knowledge for conducting clinically based concurrent and retrospective reviews of inpatient medical records • Evaluate the documentation of clinical services by identifying opportunities for improving the quality of medical record documentation • Facilitate and obtain appropriate physician documentation for clinical conditions or procedures • Participate in ongoing documentation improvement initiatives

Role Description We are seeking a per diem Clinical Documentation Specialist to join the Utilization Management department supporting Mass General Brigham Home Care. The Clinical Documentation Improvement (CDI) Specialist is responsible for enhancing the accuracy, completeness, and quality of clinical documentation to support appropriate reimbursement, quality care initiatives, and compliance with regulatory requirements. - Review patient medical records to ensure clinical documentation is accurate, complete, and compliant with established documentation standards. - Collaborate with physicians, nurses, and other healthcare professionals to clarify documentation and obtain information necessary to support accurate coding and billing. - Provide guidance to coding staff on documentation requirements that support accurate code assignment, regulatory compliance, and appropriate reimbursement. - Identify documentation gaps, trends, and opportunities for improvement, and develop strategies to enhance documentation quality and consistency. - Educate clinical staff on documentation best practices, regulatory requirements, and the impact of documentation on patient care, quality reporting, and reimbursement. - Ensure clinical documentation complies with applicable regulatory standards, including CMS guidelines, HIPAA regulations, and other healthcare requirements. - Analyze documentation quality and compliance data, prepare reports, and recommend process improvements to strengthen documentation practices. - Partner with interdisciplinary teams to ensure documentation accurately reflects the patient's clinical condition, care provided, and treatment outcomes. Qualifications - Bachelor's Degree Nursing required or Master's Degree Nursing preferred - Registered Nurse [RN - State License] - Massachusetts Licensure - COS-C Certified - Required - HCS-D - Certified - Required - Clinical nursing experience 2-3 years required - Clinical documentation experience 1-2 years preferred Requirements - No experience in lieu of a degree accepted Benefits - Competitive base pay - Comprehensive benefits - Career advancement opportunities - Differentials, premiums, and bonuses as applicable - Recognition programs designed to celebrate contributions and support professional growth Company Description Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham.