Pharmacovigilance and Patient Safety Associate

Job Description Pharmacovigilance and Patient Safety Associate

The Pharmacovigilance and Patient Safety Associate is responsible for the processing and management of serious adverse events, and the oversight of study patients’ safety matters. They work closely with other departments, sponsors, and investigator sites to ensure that proper plans are in place to appropriately collect and report information on Adverse Events (AEs) and Serious Adverse Events (SAEs).

The Pharmacovigilance and Patient Safety Associate is responsible for the processing and management of serious adverse events, and the oversight of study patients’ safety matters. They work closely with other departments, sponsors, and investigator sites to ensure that proper plans are in place to appropriately collect and report information on Adverse Events (AEs) and Serious Adverse Events (SAEs).

Additionally, they assist the department head in managing the relevant activities of the safety group.

Join a global team with more than 30 years of expertise accelerating life-changing therapies to patients worldwide.

• 105+ approved therapies for marketing applications prepared by Veristat
• 480+ oncology projects in the past 5 years
• 350+ rare disease projects delivered in the past 5 years
• Flexible, inclusive culture — 70% remote workforce, 66% women-led teams
• Learn more about our core values here!

The estimated hiring range for this role is $74K – 85K plus applicable bonus. This hiring range is specific to the USA and will vary for other regions based upon local market data. Final salary is ultimately decided upon taking into account a wide range of factors, including but not limited to: skills and experience, licensure and certifications, education, specific location and dynamic market data.

• Benefits vary by location and may include:
• Remote working
• Flexible time off
• Paid holidays
• Medical insurance
• Tuition reimbursement
• Retirement plans

• Bachelor’s Degree in a science or related field required; advanced degrees (PharmD, MD, etc.) strongly preferred.
• 2-4 years of pharmacovigilance and/or drug safety experience in a CRO, pharmaceutical, or clinical trial environment required.
• Proficient with International Conference on Harmonisation (ICH) Good Clinical Practice (GCP) guidelines and other applicable regulatory rules and guidelines as well as of medical terminology, clinical trials, and clinical research.
• Excellent project management skills, written and oral communication, organizational, and interpersonal skills are required.
• Familiarity with and ability to effectively utilize safety databases.
• Proficiency in English (written and verbal) required.
• Action-oriented and resilient in a fast-paced environment and with the ability to build and lead effective project teams, motivate others, delegate, and make and implement decisions.
• Ability to build and maintain trust and confidence and communicate effectively with client, external vendors, and internal team members.
• Ability to mentor and delegate.

Automated Decision Making:
All applicants are reviewed by a member of the Veristat Talent Acquisition team;
Veristat does not utilize an automated decision-making process.

Veristat is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.