Safety Associate

DURHAM (US)HYBRIDPOSTED: 6/24/2026
PHARMAFull-time
HIRING ORGANIZATIONIQVIAHealthcare Technology & Contract Research
Iqvia

ROLE DEFINITION & RESPONSIBILITIES

Job Overview

Review, assess and process Safety data and information, across service lines, received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations SOPs and internal guidelines under guidance and support of senior operation team members.

Essential Functions

To Prioritize and complete the assigned trainings on time.

Process Safety data according to applicable regulations, guidelines, Standard Operating procedures (SOPs) and project requirements.

To perform Pharmacovigilance activities per project requirement including but not limited to, collecting and tracking incoming Adverse Events(AE)/endpoint information determining initial/update status of incoming events database entry coding AE and Products, writing narratives, Literature related activities as per internal/ project timelines.

Creating, maintaining and tracking cases as applicable to the project plan.

Identify quality problems, if any, and bring them to the attention of a senior team member.

To mentor new teams members, if assigned by the Manager.

Attend project team meetings and provide feedback to operations manager on any challenges/issues or successes.

Qualifications

High School Diploma or equivalent Scientific or healthcare discipline or allied life sciences background with 1-1.5 years of relevant experience.

Good knowledge of medical terminology.

Working knowledge of applicable Safety Database (ARGUS).

Good working knowledge of Microsoft Office and web-based applications.

Ability to multi-task, manage competing priorities and deadlines.

Willingness and aptitude to learn new skills across Safety service lines.

Ability to work as a Team Player, contribute and work towards achieving Team goals.

Ensure quality of deliverables according to the agreed terms.

Use of telephone and face-to-face communication requiring accurate perception of speech.

May require occasional travel.

May require on-site work (in a hybrid capacity, 1 day a week)

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at  https://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $44,900.00 - $112,100.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

REQUIRED VERIFIED SKILLS

Pharmacovigilance
Clinical Research
Microsoft Office
SOP
Safety Database

COMPENSATION & REWARDS

Salary: Competitive / Disclosed upon candidate shortlisting
Salary for this Safety Associate position is competitive and aligned with industry standards for this location.

ORGANIZATION CONTEXT & CULTURE

IQVIA is a leading global provider of advanced analytics, technology solutions, and contract research services (CRO) to the life sciences industry. The company helps pharmaceutical, biotech, and medical device clients accelerate the development and commercialization of new medical treatments through its extensive data, technology, and human expertise. Their offerings span from clinical trial design and execution to real-world evidence and commercial effectiveness.

TEAM SIZE: 87,000+ employees
INDUSTRY: Healthcare Technology & Contract Research

EXPECTED CAREER ROADMAP

Career path typically progresses from Associate, to Senior Specialist, and eventually to Manager or Lead positions within the department.

APPLICATION ADVISORY

Ensure your resume clearly showcases experience with: Pharmacovigilance, Clinical Research, Microsoft Office. Prepare real-world examples demonstrating these skills for the interview.
RECOMMENDED TRAINING
1/5

READY TO SUBMIT?

Verify your capability profile and matching credentials before submitting direct applications.