• Supports the medical business goals and objectives of one of Sobi’s rheumatology products, providing strategic leadership and tactical execution • Provide strategic and scientific medical affairs leadership for a Rheumatology product in development • Help develop and implement the US medical strategy, tactical plans, and HCP engagement plans • Partner with field medical to engage and educate health care providers (HCPs), medical organizations, payers, and patient advocacy groups • Represent the overall Medical Science organization on cross-functional initiatives as required • Provide feedback and insights to medical affairs deliverables, and cross-functional partners, including the design and implementation of Medical Affairs plans • Develop/enhance KOL and key institution engagement plans, and participate in KOL engagement and development • Help plan and execute advisory boards and educational activities (webinars, medical roundtables, symposium, congress presence) • Collaborate closely with global medical and clinical colleagues, ensuring the US perspective and insights are incorporated into global initiatives

Role Description TISTA is seeking a detail-oriented Medical Record Abstractor to support healthcare quality improvement initiatives. In this role, you will: - Review medical records and source documentation to identify and abstract required clinical data elements. - Accurately enter abstracted data into designated abstraction software systems. - Maintain the confidentiality and security of medical records and protected health information (PHI). - Follow established processes, procedures and quality standards. - Meet or exceed established productivity and accuracy expectations. - Perform additional project-related duties as assigned. Qualifications - Minimum of two (2) years of experience in a hospital, healthcare or medical record review environment. - Education or formal training in a related field may substitute for experience requirements. - Thorough knowledge of medical terminology. - Proficiency with Microsoft Office applications. - Strong attention to detail with the ability to perform work accurately and efficiently. - Ability to prioritize and manage multiple tasks in a fast-paced environment. - Ability to work independently and collaboratively within a team environment. - Must be able to obtain and maintain a Public Trust clearance. Requirements - Preferred Qualifications: - Minimum of 1-2 years of hands-on clinical data abstraction. - Familiarity with healthcare quality measures and chart review methodologies. - Proven ability to meet strict daily chart-volume quotas and accuracy standards. Education - High school diploma or equivalent required. Location - Remote, USA. Pay Range The pay for this position ranges from $40,730 to $47,500. The actual salary offer will carefully consider a wide range of factors, including your skills, qualifications, experience, and location. Also, certain positions are eligible for additional forms of compensation, such as bonuses. Benefits - Above Industry Healthcare Benefits - Remote Working Options - Paid Time Off - Training/Certification opportunities - Healthcare Savings Account & Flexible Savings Account - Paid Life Insurance - Short-term & Long-term Disability - 401K Match - Tuition Reimbursement - Employee Assistance Program - Paid Holidays - Military Leave - And much more!

Role Description Due to the expanding portfolio, we are looking for Medical Directors to join our clinical teams in late development oncology at Astellas. - Core member of the clinical team responsible for the design and execution of one or more clinical trials. - Serves as Medical Monitor with responsibility for safety monitoring on clinical studies. - Generates safety-related documents, such as medical monitoring reports. - Collaborates closely with the safety officer in writing and/or reviewing safety narratives, investigator letters, and other safety documentation for site-reported safety events. - Responsible for the medical aspects of all study-related documents, including clinical study protocol, informed consent forms, clinical database, safety committee charters, and clinical study reports. - Works with Development Scientists and Clinical Operation Leads to ensure efficient execution of clinical trials and acquisition of high-quality clinical data. - Supports functional level clinical development related initiatives as needed. - Leads and/or participates in scientific and medical training for team members and external clients, investigators, and site staff. - Reports to the Global Medical Portfolio Lead for Late Oncology. Qualifications - MD or MD/PhD - 5+ years experience in oncology clinical trial design and execution in a bio-pharmaceutical development organization or a balance of experience at an academic institution and a pharmaceutical company. - Excellent verbal and written communication skills in English. - Experience working in global teams and a global matrixed, remote working environment. - Aware of cultural diversity and how to influence and manage in a multi-cultural organization. - Highest level of scientific integrity and impeccable work ethics. Requirements - Board certified in Oncology or Oncology-related specialty (preferred). - Experience in solid tumors, preferably Gastro-Intestinal, Thoracic or Genito-Urinary (preferred). - Experience in late development oncology (Ph3) (preferred). - Direct experience leading global regulatory marketing authorization submissions and defense of those submissions (preferred). Benefits - Medical, Dental and Vision Insurance - Generous Paid Time Off options, including Vacation and Sick time, plus national holidays including year-end shut down - 401(k) match and annual company contribution - Company paid life insurance - Annual Corporate Bonus and Quarterly Sales Incentive for eligible positions - Long Term Incentive Plan for eligible positions - Company fleet vehicle for eligible positions - Referral bonus program

Role Description As our Medical Records Professional, you will ensure the integrity, confidentiality, and accessibility of patient health information, meticulously managing records in compliance with all regulatory standards and organizational policies. Every day you will: - Accurately process, retrieve, and maintain patient medical records (electronic and paper). - Manage requests for Protected Health Information (PHI) ensuring strict HIPAA compliance. - Play a key role in ensuring the completeness, accuracy, and proper indexing of health information within the EHR system. - Demonstrate meticulous attention to detail, strong organizational skills, and proficiency with EHR systems. - Manage incoming departmental telephone calls and faxes and respond as appropriate. - Maintain accurate physician contact lists. - Perform miscellaneous clerical duties based on departmental needs, such as departmental mail distribution, filing, sorting, copying, record keeping, posting, tabulating information, and organizing assigned tasks. - Maintain supply of documentation materials. - Deliver and pick up records, interoffice mail, etc. as needed. - Prepare and mail all outgoing patient correspondence and appropriate attachments. Qualifications - Strong understanding of medical terminology. - Knowledge of health information management principles. - Comprehensive knowledge of HIPAA and privacy regulations. - Meticulous attention to detail. - Strong organizational skills. - Proficiency with EHR systems. Requirements - High School Diploma or GED. - One (1) year clerical experience. - Familiarity with applicable alphabetic and numeric filing systems.