• Support 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. • Develop a US evidence generation strategy to address stakeholder (HCPs, payers, and patients) needs. • Oversee any medical affairs-led research initiatives, including US Phase IV clinical programs.

• 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