Pharmacovigilance Job at ICON | Apply Now
Looking for a pharmacovigilance job in the healthcare and clinical research industry? ICON is hiring a Graduate Pharmacovigilance Associate for a remote, home-based role in Mexico City. This opportunity is ideal for life sciences graduates who want to begin their career in drug safety, adverse event reporting, and regulatory compliance while working with one of the world’s leading clinical research organizations.
- Job Position: Graduate Pharmacovigilance Associate
- Company Name: ICON
- Job ID: JR144702
- Location: Mexico City, Mexico – Home Based / Remote Job (CDMX)
- Employment Type: Full-Time
- Job Category: Drug Safety | Pharmacovigilance | ICON Careers
About the Company
ICON plc is a world-leading healthcare intelligence and clinical research organization. The company supports pharmaceutical, biotechnology, and medical device organizations through innovative clinical development solutions. ICON is known for creating an inclusive work environment, promoting professional growth, and helping employees build successful long-term careers in the healthcare industry. Through ICON careers, graduates and professionals gain access to global opportunities, training, and career development.
Job Description
ICON is currently seeking a Graduate Pharmacovigilance Associate to join its diverse and dynamic team. This pharmacovigilance job is home based in Mexico City and is a great opportunity for recent graduates who want to build a career in drug safety and regulatory affairs.
As a Graduate Pharmacovigilance Associate at ICON, you will support the safety monitoring and reporting of pharmaceutical products. You will contribute to ensuring the safety and efficacy of therapies by assisting in the collection, analysis, and communication of safety data in compliance with regulatory requirements.
Qualifications
- Bachelor’s degree in life sciences or a related field.
- Strong attention to detail and excellent organizational skills.
- Ability to manage multiple tasks and prioritize effectively.
- Excellent communication and interpersonal skills.
- Ability to work collaboratively in a team environment.
- Basic understanding of pharmacovigilance principles and regulatory guidelines is desirable, but not required.
- Relevant training will be provided by ICON.
- Proficiency in Microsoft Office applications.
- Good analytical and problem-solving skills.
Skills Preferred
- Knowledge of adverse event reporting
- Interest in clinical research and drug safety
- Time management and multitasking skills
- Strong written and verbal communication
- Team collaboration and analytical thinking
Key Responsibilities
- Support the collection, review, and processing of adverse event data according to pharmacovigilance regulations and company procedures.
- Assist in the preparation and submission of safety reports to regulatory authorities and stakeholders.
- Collaborate with cross-functional teams to ensure timely and accurate communication of safety information.
- Contribute to the development and maintenance of pharmacovigilance documentation, including standard operating procedures and safety management plans.
- Participate in training and development activities to gain a deeper understanding of pharmacovigilance practices and regulatory requirements.
- Maintain organized records and manage multiple tasks effectively in a fast-paced work environment.
If you are searching for a pharmacovigilance job that offers training, growth, and the chance to work with a global organization, the Graduate Pharmacovigilance Associate role at ICON is an excellent opportunity. Apply today and take the first step toward building your future in drug safety and clinical research with ICON careers.
