Pharmacovigilance and Patient Safety Associate

Veristat, LLC; United States; Remote; USD 74,000 - 85,000; Full time

Benefits offered by this job

Remote working

Flexible time off

Paid holidays

Medical insurance

Tuition reimbursement

Retirement plans

Job summary

Veristat, LLC is seeking a Pharmacovigilance and Patient Safety Associate to manage SAEs and safety matters across clinical studies. The role involves collaboration with sponsors, investigator sites, and internal teams to ensure accurate AE/SAE reporting and to support safety training programs.

The position emphasizes strong project management and clear communication in a fast-paced environment, with a mostly remote work arrangement and comprehensive benefits.

Qualifications

• Bachelor’s degree in science or related field required.
• 2-4 years pharmacovigilance/drug safety experience required.
• Proficient with GCP/ICH guidelines and regulatory rules.

Responsibilities

• Process and manage serious adverse events (SAEs) and safety matters for studies.
• Assist in developing and implementing safety training programs.
• Support department head in safety group activities.

Skills

Project management

Written and verbal communication

Organizational skills

Interpersonal skills

English proficiency

Education

Bachelor’s degree in science or related field

Advanced degrees (PharmD, MD) preferred

Tools

Safety databases

Job description

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 facilitating the development and implementation of training programs for internal and external personnel involved in managing safety information. Additionally, they assist the department head in managing the relevant activities of the safety group.

Make an Impact at Veristat! 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!

What we offer:

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

What we look for:

• 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. #LI-SI1

Veristat is an equal opportunity employer.

We celebrate diversity and are committed to creating an inclusive environment for all employees.

We are an Equal Opportunity Employer that values the strength and creativity that diversity brings to our workplace.

Veristat provides equal employment opportunities to all employees and applicants for employment without regard to age, disability, genetics, gender identity or expression, gender reassignment (i.e., transgender status), marriage and civil partnership, pregnancy and maternity, race (including color, nationality, and ethnic or national origins), religion or belief, sex or sexual orientation, physical appearance, veteran status, source of income, arrest or conviction record or any other category protected under characteristics considered unlawful in any circumstances of employment offers and practices.

Reasonable Accommodations

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If you require a reasonable accommodation to complete your application, participate in an assessment, or attend an interview, please contact our Talent Acquisition team at [e-mail] or [phone].

We will work with you to meet your needs, ensuring a fair process.

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