Sr. Medical Director, Drug Safety and Pharmacovigilance - Remote - United States

Praxis Precision Medicines Inc has an opening for a Senior Director SafetyPharmacovigilance in Boston MA 40 hoursweek 5% shortterm travel including up to 1% international travel and 4% domestic Remote telecommuting position can work from anywhere within the US · ...

We are focused on advancing first- or best-in-class medicines for childhood and adult diseases with equal intensity. We were founded to address the lack of new therapies resulting from the traditional drug development model, that has left children with cancer and their families w ...

Join us as we transform immunology and deliver medicines that help autoimmune patients get their lives back. · ...

BridgeBio is pioneering a "moneyball for biotech" approach by pooling projects and promising early-stage research from academia together under one financial umbrella to reduce risk and unleash innovation. · Responsibilities · Supporting Pharmacovigilance and R&D IT systems includ ...

+Join us as we transform immunology and deliver medicines that help autoimmune patients get their lives back. · +We are building a new kind of biotech company, one that maintains its roots as a science-based start-up and pushes our commitment to innovate across all corners of our ...

Job summaryThe Senior Manager Pharmacovigilance will be responsible for collecting and managing adverse events reports from internal or external sources. · ...

The Executive Medical Director will lead and oversee a team of Product Safety Physician Leads within assigned franchise or disease area. · ...

We build bridges to groundbreaking advancements in rare disease, and develop life-changing medicines for patients with unmet needs as fast as humanly possible. · In collaboration with internal and external stakeholders establish the safety strategy for the clinical development an ...

The Sr. Medical Director, Drug Safety is responsible for the overall risk management and safety strategy of assigned products. · Oversight and understanding of all aspects of the assigned product's safety profile from clinical development to post-approval safety surveillance. · C ...

We pioneer a "moneyball for biotech" approach, pooling projects and promising early-stage research together under one financial umbrella to reduce risk and unleash innovation. · ...

We are seeking an experienced professional to contribute to our safety and regulatory data analytics initiatives. · ...

We are passionate about creating an inclusive workplace that promotes collaboration integrity and excellence As we expand we seek the most talented individuals with diverse backgrounds cultures perspectives and experiences to join our team. · ...

BridgeBio is a biotech company that pioneers a "moneyball for biotech" approach, pooling projects and promising early-stage research from academia together under one financial umbrella to reduce risk and unleash innovation. They build bridges to groundbreaking advancements in rar ...

+Job summary · MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for central nervous system disorders. · +Provide overall leadership and management of a cross-functional development team, accountable for the development of a promising compou ...

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. · ...

Lead the Central Statistical Monitoring (CSM) team within the Global Statistics department to support the RBQM: providing statistical design, interpretation and governance for monitoring activities that protect subject safety ensure data integrity and support trial reliability ac ...

This leadership role is responsible for developing and implementing global regulatory strategies for clinical investigational studies and commercialization of vaccines for both adult and pediatric populations. · Bachelor’s degree in a relevant scientific or technical discipline. ...

The Clinical Research Associate responsibilities will be dependent upon the type and timing of the program to which the CRA is assigned and will typically include activities involving start-up and study implementation, on-site monitoring of clinical research studies as well as on ...

We are seeking an Associate Director of Clinical Quality Assurance (CQA) Auditor who will serve as the primary auditor for GCP/GLP/GVP audits and oversee quality activities including leading and conducting internal and external audits.Serve as CQA audit program process owner. · L ...

The Executive Director, Clinical Development will lead clinical development of at least one high impact project. · (Provide leadership and clinical oversight for all assigned studies and programs) · ...