Pharmacovigilance Scientist

Tonix Pharmaceuticals* is a fully integrated, commercial-stage biotechnology company focused on central nervous system (CNS) and immunology treatments in areas of high unmet medical need. TONMYA® (cyclobenzaprine HCl sublingual tablets 2.8 mg) is the first new treatment for fibromyalgia in adults in more than 15 years. Tonix’s CNS commercial infrastructure supports its marketed products, including its acute migraine products, Zembrace® Symtouch® (sumatriptan injection 3 mg) and Tosymra® (sumatriptan nasal spray 10 mg). Tonix is investigating TONMYA® in Phase 2 clinical trials to evaluate its potential in major depressive disorder and acute stress disorder/acute stress reaction. Tonix is also advancing a pipeline of immunology programs, including TNX-4800, a Phase 2 ready long-acting human anti- Borrelia  OspA monoclonal antibody (mAb) for the prevention of Lyme disease in the U.S., and TNX-1500, a Phase 2 ready third-generation CD40 ligand inhibitor for the prevention of kidney transplant rejection. In addition, the Company is progressing TNX-2900 (intranasal potentiated oxytocin), which is Phase 2 ready for the treatment of Prader-Willi syndrome, a rare disease. To learn more, visit  www.tonixpharma.com  and follow the Company on  LinkedIn  and  X . *Tonix’s product development candidates are investigational new drugs or biologics; their efficacy and safety have not been established and have not been approved for any indication. Zembrace SymTouch and Tosymra are registered trademarks of Tonix Medicines. TONMYA is a registered trademark of Tonix Pharma Limited. All other marks are property of their respective owners. Position Overview Tonix is seeking an experienced Pharmacovigilance Scientist to join our Drug Safety and Pharmacovigilance team. Reporting to the Associate Director, Drug Safety and Pharmacovigilance this role is pivotal in ensuring the safety profiles of our products are effectively monitored and assessed. The PV Scientist will play a key role in cumulative safety data reviews, safety surveillance, and regulatory reporting. Essential Duties Perform cumulative safety data reviews across trials or programs to assess safety profiles and identify emerging risks or trends Coordinate and document ongoing safety surveillance activities. Activities will include safety data review, signal validations, signal evaluations, literature reviews Lead aggregate report (PSUR/PADER/DSUR) activities, including vendor oversight and project management, database requests, data analysis, report authoring, and quality checks Manage literature review plan for assigned product(s) and provide feedback to vendor on routine literature surveillance activities Coordinate responses for ad hoc safety queries (eg, health authority requests) in collaboration with the cross functional team members, as needed. Perform safety data analyses, draft query responses, and prepare documents for cross functional review and finalization Represent safety at cross functional product meetings For investigational product(s): Support activities relevant to investigational program including (but not limited to): Routine/ad hoc updates to safety content of Investigator Brochure (IB), safety content of protocols, CRFs, ICFs Ongoing data review, including lab, vitals, ECG, and AE data review Review preliminary data and prepare presentations for safety review committees Maintain strong working knowledge of relevant regulations associated with the above activities Contributes to initiatives for process improvement and cross-product process consistency Other tasks as assigned or required Necessary Skills and Abilities Demonstrated experience in analysis and interpretation of medical and scientific data and excellent verbal and written skills Demonstrated ability to work effectively either independently or collaboratively in a team environment (including Safety, Clinical Development, Medical Affairs, Clinical Operations, and Regulatory), as well as with external colleagues Demonstrated ability to prioritize multiple assignments and proactively identify solutions, as needed Strong organizational, project management and leadership skills: Leads and conducts (independently and/or collaboratively) all aspects of substantive projects such as signaling, authoring of aggregate data reports, and responses to regulatory agency requests. Scientifically sound and clinically accurate approaches to interpret data involving patient safety. Familiarity with pharmacovigilance and drug development, including knowledge of applicable clinical trial safety regulations and post-marketing safety regulations. Includes familiarity with case processing, expedited reporting rules, and safety database concepts Strong knowledge of common data processing software (EXCEL, PowerPoint, Microsoft Word, Business Objects), MedDRA, and Argus Safety System Education and Experience Requirements Advanced degree in a relevant healthcare or life sciences field (e.g., PharmD, MD, PhD, MPH, or equivalent clinical degree such as RN or NP). Minimum 5 years relevant medical, scientific/clinical, or pharmaceutical experience, including 3 years of experience in drug safety serving in a PV Scientist role Salary Range $116,000 — $170,000 USD * Please note that Tonix does not offer sponsorship for this role. Recruitment & Staffing Agencies Tonix does not accept agency resumes unless contacted directly by internal Tonix Talent Acquisition. Please do not forward resumes to Tonix employees or any other company location; Tonix is not responsible for any fees related to unsolicited resumes. Compensation & Benefits Tonix provides a comprehensive compensation and benefits package which includes: Medical, Dental & Vision Insurance, Basic and Voluntary Life and AD&D Insurance, Short- and Long-Term Disability Insurance, Flexible Spending Accounts, Health Savings Account, and Employee Assistance Programs Pet