Associate Director, Global Patient Safety Operations at Ironwood Pharmaceuticals

Boston, Massachusetts, United States -

Full Time

Start Date

Immediate

Expiry Date

15 Apr, 26

Salary

199500.0

Posted On

15 Jan, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Case Processing, Vendor Management, Safety Reporting, Regulatory Compliance, Clinical Trials, Data Handling, Safety Databases, Performance Metrics, Inspection Readiness, Safety Management Plan, MedDRA Terminology, Quality Assurance, Alliance Management, Project Management, Training, Guidance

Industry

Biotechnology Research

Description

Ironwood Pharmaceuticals is a leading gastrointestinal (GI) healthcare company on a mission to advance the treatment of GI diseases and redefine the standard of care for GI patients. One of the focus areas is on discovering, developing, and commercializing innovative treatments for patients with severe, rare conditions for which there is a significant unmet medical need. These conditions are challenging to diagnose, often devastating, and have limited, if any, treatment options. The lead product candidate, apraglutide, is a next-generation, best-in-class, synthetic peptide analog of glucagon-like peptide-2, or GLP-2, and is in Phase 3 for the treatment of patients with short bowel syndrome, or SBS, a malabsorption disorder caused by the loss of functional small intestine. It is an exciting time to join as Phase 3 is underway and the company is preparing for an initial launch in the coming years. Position Summary: As a key member of Global Patient Safety Operations, the Associate Director, GPS Ops, is responsible for operational management and oversight of case processing activities, vendor management and supporting functions such as alliance management, quality & compliance, and safety systems. The incumbent will join the Global Patient Safety Operations department reporting directly to the Vice President, Global Patient Safety. Responsibilities: Provide oversight of operational and case management activities for safety reporting for both investigational and marketed products Managing Case Processing Vendor including oversight of daily responsibilities, providing guidance, training, and evaluating vendor performance and quality of work Generate performance and compliance metrics for the PV vendor and monitor for trends and possible improvements Identify and lead needed upgrades to Safety Database functionality in conjunction with Vendor, IT and project management colleagues Lead and provide safety operations support to Clinical Trial Teams (CTT) on assigned studies including input to protocols, IBs, CSRs and other relevant study documents Develop documents related to safety case processing and reporting such as Safety Management Plan, Safety Reporting Forms and completion guidelines, reconciliation plan, data handling conventions, blinding and unblinding protections and SOPs Review new or updated PV regulations to identify required modifications to internal Ironwood procedures and/or agreements with vendors or business partners Maintain inspection readiness and collaborate with internal teams and vendors to prepare for Regulatory Authority inspections and internal/external audits as subject matter expert for PV operations Contribute to responses to safety requests from Regulatory Authorities and internal teams Required Qualifications: Bachelor's degree in life sciences; A health professional degree (e.g., PharmD, BSN, RN, MPH) is preferred. 7-10 years of relevant experience that includes experience in case processing for US and EU clinical trials. Strong working knowledge of global safety regulations for regulatory authorities such as of FDA, MHRA, EMA (GVP), ICH Guidelines and their specific implications to case processing, patient privacy, and safety databases. Experience with clinical trial data and safety reporting tools such as Argus Safety, Electronic Data Capture, electronic reporting gateways, elluminate platform Knowledge of MedDRA terminology and its application, and principles of data entry and data extraction with global safety databases Ironwood currently anticipates that the initial base salary for this position could range from between $167,000 to $199,500. The actual base salary will depend, in part, on the successful candidate’s qualifications for the role, including education and experience. Ironwood offers a comprehensive compensation and benefits program to eligible employees, including Restricted Stock Unit awards; eligibility to participate in either a bonus or sales incentive program; company-sponsored 401(k) with matching contributions; eligibility for medical, dental, vision and prescription drug benefits; wellness stipends; and a generous vacation/holiday schedule. #LI-Hybrid

Responsibilities

The Associate Director is responsible for operational management and oversight of case processing activities and vendor management. They will also lead safety operations support for Clinical Trial Teams and ensure compliance with safety reporting regulations.