Job Title: Pharmacovigilance Project Manager
Job Location: Cambridge, MA, USA
Job Location Type: Remote
Job Contract Type: Full-time
Job Seniority Level: Mid-Senior level
Posted: 18 February 2025
Job Type: Permanent
Reference: 954319
Job Description
Title: Pharmacovigilance Project Manager
Location: Remote role, EST hours
Duration: 06 Months (Possible Extension)
Pay rate: $60 – $73 /Hr
Top 3 Skills:
* PV CRO management
* Audit and inspection readiness
* PV process improvement
Experience:
* Minimum 4 years pharmaceutical or health care related industry experience
Required:
* Minimum 3 years PV experience with 1 year experience working with CROs, vendors, and relationship management required
* Global experience with CROs, vendors and relationship management
Education:
* Bachelors required. Advanced degree in scientific/medical field.
* Good cross cultural understanding and experience.
* Experience in people management and well developed skills in teambuilding, motivating and developing people.
* Demonstrated skills in negotiation and consensus decision making.
* Critical thinking and analytical skills and ability to make key decisions.
* Demonstrated effectiveness in external partner relationship management.
* Understanding of medical/scientific terminology.
* Good knowledge of PV regulations for the global pre-and post-market, i.e. FDA, EMA, ICH GVP.
* Experience with safety databases, including MedDRA and WHO Drug.
* Excellent written/oral communication skills.
* Accuracy and attention to detail.
* Flexible mindset.
* Team worker with collaborative approach.
* Ability to prioritize under pressure.
* Well developed organizational skills.
Objectives:
* Serve as a primary liaison and point of contact for vendor operations and vendor oversight, including vendors performing case management, case intake (i.e., Call Centers), scientific literature review, etc.
* Oversee operations performed by the PV BPO vendor including contract compliance, quality and timeliness of deliverables.
* Provide Subject Matter expertise (SME) during audits and inspections in the areas of case processing/case management activities, literature monitoring, legal case processing, vendor oversight, etc.
Accountabilities:
* Provide leadership and oversight on case management for the Global PV Operations Team to ensure adverse event information is processed according to company timelines and quality standards.
* Oversee regulatory submissions for ICSRs from the Global Safety database, on-time delivery of adverse event reports to global Health Authorities, alliance partners, local operating companies (LOCs) including SUSAR and SAE communication to ECs and investigators as applicable.
* In partnership with the Global Standards and Compliance team, direct and manage communication with alliance partners, LOCs and CROs regarding the evaluation and processing of ICSRs.
* In partnership with the Global Standards and Compliance team, lead and direct the review and approval of alliance partner safety data exchange agreements for the appropriate safety reporting requirements.
* Ensure overall performance of the department and compliance with global regulatory requirements by implementation of appropriate SOPs, processes, metrics, and monitoring of performance and compliance, and training at a global level.
* Oversee and direct reconciliation processes for case exchange with LOCs and alliance partners.
Dexian is a leading provider of staffing, IT, and workforce solutions with over 12,000 employees and 70 locations worldwide. As one of the largest IT staffing companies and the 2nd largest minority-owned staffing company in the U.S., Dexian was formed in 2023 through the merger of DISYS and Signature Consultants. Combining the best elements of its core companies, Dexian’s platform connects talent, technology, and organizations to produce game-changing results that help everyone achieve their ambitions and goals.
Dexian is an Equal Opportunity Employer that recruits and hires qualified candidates without regard to ancestry, citizenship, or veteran status.
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