Remote Life Science Job at ICON Mexico
Are you searching for a remote life science job that allows you to start a career in drug safety and clinical research? ICON plc careers offer an exciting opportunity for graduates to work as a pharmacovigilance associate in Mexico City. This job in Mexico provides early-career professionals with the chance to support safety monitoring of pharmaceutical products while gaining valuable experience in regulatory compliance and adverse event reporting. It is an excellent job opportunity for Life Science graduates interested in pharmacovigilance, drug safety, and global clinical research operations.
About the Company
ICON plc is a global healthcare intelligence and clinical research organization that supports the development of life-saving medicines and medical devices. With operations in multiple countries, ICON plc careers provide opportunities for professionals to contribute to clinical trials, drug safety monitoring, and regulatory research. The company works with leading pharmaceutical, biotechnology, and medical device organizations worldwide. Through positions such as pharmacovigilance associate, ICON plc helps professionals build meaningful careers in clinical research and global healthcare innovation.
Job Details:
- Job Title: Graduate Pharmacovigilance Associate
- Job Id: JR142421
- Location: Mexico City (Home-Based – CDMX)
- Company: ICON plc – Drug Safety, ICON Strategic Solutions (Remote)
About the Pharmacovigilance Associate Role
The Graduate Pharmacovigilance Associate supports the safety monitoring and reporting of pharmaceutical products within ICON’s Drug Safety team. The role contributes to ensuring the safety and effectiveness of therapies by assisting with the collection, analysis, and communication of safety data.
The associate works in compliance with global pharmacovigilance regulations and company procedures while collaborating with cross-functional teams. The position provides an opportunity to gain practical experience in pharmacovigilance within a global clinical research environment.
Key Responsibilities
- Support the collection, review, and processing of adverse event data according to pharmacovigilance regulations and internal procedures.
- Assist in the preparation and submission of safety reports to regulatory authorities and relevant 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 (SOPs) and safety management plans.
- Participate in training and professional development activities to build knowledge of pharmacovigilance practices and regulatory requirements.
Candidate Profile
- Bachelor’s degree in Life Sciences, or a related field.
- Strong attention to detail and organizational skills, with the ability to manage multiple tasks effectively.
- Excellent communication and interpersonal skills, with the ability to work collaboratively in a team environment.
- Basic understanding of pharmacovigilance principles and regulatory guidelines is desirable but not mandatory; training will be provided.
- Proficiency in Microsoft Office applications with good analytical and problem-solving skills.
Benefits and Opportunities for Remote Life Science Job
- Competitive salary and benefits package.
- Annual leave entitlements depend on the country’s policy.
- Health insurance options for employees and their families.
- Retirement planning programs to support long-term financial security.
- Access to the Global Employee Assistance Programme (LifeWorks) provides 24/7 support from a network of specialized professionals.
- Life assurance coverage.
- Additional flexible benefits such as childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, and health assessments, depending on country availability.
