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Full-time
bachelor degree
Competitive base salary, Performance related incentives, Medical coverage, Dental coverage, Vision coverage, Retirement plans
Posted 6d ago
~40 hrs/week
Remote in Mexico
Responsibilities
The Senior Clinical Associate oversees and supports the execution of clinical trials to ensure adherence to protocols, regulatory requirements, and project timelines. They manage site activities, provide guidance to clinical staff, and collaborate with cross-functional teams to optimize processes and mitigate risks.
Requirements
Candidates must hold a bachelor's degree in a scientific or healthcare-related field and possess significant experience in clinical trial management. Strong organizational, problem-solving, and communication skills are required to work independently and guide others effectively.
Full job description
Mexico. Home based.
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As a Senior Clinical Associate at ICON, you will oversee and support the execution of clinical trials, ensuring the highest standards of quality, compliance, and efficiency.
What You Will Do:
You will lead on clinical coordination tasks requiring technical depth, with a focus on quality and continuous improvement.
Key responsibilities include:
Managing and coordinating clinical trial activities to ensure adherence to protocols, regulatory requirements, and project timelines.
Collaborating with cross-functional teams to address clinical trial issues, optimize processes, and ensure the effective execution of studies.
Overseeing site management and monitoring to ensure data integrity and compliance with study protocols.
Providing guidance and support to clinical staff and investigators, ensuring adherence to best practices and regulatory standards.
Tracking and reporting on trial progress, identifying potential risks, and implementing strategies to mitigate challenges.
Your Profile:
You will have a strong foundation in clinical coordination, with the experience to work independently and guide others.
Required qualifications and experience:
Bachelor's degree in a relevant scientific discipline or healthcare-related field
Significant experience in clinical trial management, with a strong understanding of clinical trial processes and regulatory requirements.
Proven ability to manage multiple projects effectively, with strong organizational and problem-solving skills.
Excellent communication and interpersonal skills, with the ability to collaborate effectively with diverse teams and stakeholders.
Detail-oriented with a proactive approach to ensuring trial success and addressing clinical challenges.
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply
Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times.
We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.
Offices: ICON plc, South County Business Park, Leopardstown, Dublin, D18 X5R3, IE · 123 Smith Street, Farmingdale, New York NY 11735, US · Block 2, Hamilton House, National Technology Park, Limerick, V94 TRW8, IE · 100 Longwater Avenue, Green Park, 3rd Floor, North and South Wings, Reading, England RG2 6GP, GB · 1 Almondview Office Park, West Lothian, Livingston, EH54 6SF, GB
Medical DeviceTherapeuticsGovernment and Public Health SolutionsClinical Research ServicesCommercialisation and OutcomesOncologyValue Based HealthcareClinical TrialsPatient RecruitmentInnovation
How many Science & Research jobs are open in São Paulo, Brazil right now?
There are currently 426 open science & research positions in São Paulo, Brazil listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Science & Research roles in São Paulo, Brazil?
Companies currently hiring include ICON plc, Anton Paar, IQVIA, Zoetis, Thermo Fisher Scientific, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Science & Research jobs in São Paulo, Brazil?
Yes — 213 of the 426 open science & research positions offer remote or hybrid work (107 remote, 106 hybrid).
How do I apply for Science & Research jobs in São Paulo, Brazil?
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.