• Performs quality assurance review of reports, correspondences, addendums or supplemental reviews • Ensures clear, concise, evidence-based rationales have been provided in support of all recommendations and/or determinations • Ensures that all client instructions and specifications have been followed and that all questions have been addressed • Verifies that the peer reviewer has attested to only the fact(s) and that no evidence of reviewer conflict of interest exists • Assists in resolution of customer complaints and quality assurance issues as needed

• Ensure reports are of the highest quality and integrity • Assist with quality assurance questions • Perform quality assurance review of reports and correspondences • Verify board specialty reviews compliance • Resolution of customer complaints and quality assurance issues

Role Description This is a remote position. As a Global Drug Safety Associate , you will support the delivery of high‑quality clinical and post‑marketing safety activities. You will work closely with senior Drug Safety colleagues to process safety cases, maintain documentation, and support compliance and operational tasks across multiple projects. Key Responsibilities - Support the processing of safety cases from clinical trial and post‑marketing sources, including AEs, SAEs, and SUSARs. - Assist with case receipt, triage, data entry, MedDRA and WHO Drug coding, follow‑up activities, and quality checks within safety databases. - Support expedited and local ICSR submissions under supervision. - Assist with reconciliation of safety data with clinical databases. - Support global and local literature monitoring activities. - Maintain and update Drug Safety documentation, trackers, and project files in line with internal procedures. - Provide administrative and operational support to the Global Drug Safety team, including mailbox monitoring and document management. - Support compliance monitoring, reporting activities, and internal process adherence. - Collaborate with cross‑functional teams and external partners as required. Qualifications - Bachelor’s degree in pharmaceutical sciences, life sciences, medicine, or a related field. - 1–3 years of experience in Drug Safety, Pharmacovigilance, or a medical environment, including case processing and regulatory submissions. - Experience in safety case processing within both clinical trial and post‑marketing settings is required. - Basic understanding of Drug Safety regulations and guidelines, including ICH, GVP, GCP, and CIOMS. - Experience or familiarity with safety databases is an advantage. - Fluent written and spoken English. - Strong attention to detail, organizational skills, and willingness to learn. - A collaborative team player with a positive and proactive attitude. Benefits - Work remotely while contributing to a global life sciences consultancy. - Lead quality operations that directly influence patient safety and regulatory compliance. - Collaborate in a multicultural, inclusive, and innovative environment. - Enjoy opportunities for career progression, professional development, and international exposure. - Flexible Work Options: Remote working flexibility to support your lifestyle. - Generous Time Off: Enjoy 5 weeks of holiday plus national holidays and 3 personal days to recharge. - Home Office Support: Get support to create a productive home office setup. - Bonuses: Benefit from an annual bonus program, spot bonuses, and employee-nominated recognition. Company Description At Arriello, we provide Pharmacovigilance, Quality & Compliance, and Regulatory Affairs services to global pharmaceutical and life sciences companies, helping them meet regulatory requirements and protect patient safety. We are a growing business with a collaborative culture focused on high‑quality delivery, continuous improvement, and giving people the space to do their best work. Our values guide how we work: - Inclusive – We value fairness, respect, and learning from one another. - Dedicated – We deliver practical, client‑focused solutions. - Innovative – We work together to find better ways forward. - Passionate – We build strong relationships and care about the quality of what we do.

• Gather claim data and manage low to mid-level workers compensation claims to full duty Return to work • Facilitate appropriate treatment services efficiently, within required Ohio BWC Guidelines for compliance, company standards, industry best practices and/or client specific requirements • Obtain expected elements for subsequent EDI to the Bureau of Workers Compensation (BWC) • Manage medical-only and low- to mid-level lost-time workers compensation claims under close supervision • Process workers compensation claims reviewing receipt of compensation; Treatment plans; facilitating services; collaborating with all claim parties with updates and changes • Verify return to work documentation through telephonic and written communications and records return to work dates appropriately in system(s) • Manage claims in close collaboration with Claims Management Team • Support other claims management staff with larger or more complex claims as necessary • Make referral for case management and/or utilization management when work status changes due to functional limitations/medical instability • Document communications and claims management appropriately in system(s) • Respond to all inquiries within one (1) business day • Maintain knowledge of BWC rules and laws, workers compensation process, and CHS policies and procedures • Maintain professional client relationships • Meet and maintain productivity and quality expectations