CRA (Level II) in Remote, India | Clinical Research at Thermo Fisher Scientific

Role overview

CRA (Level II) in Remote, India | Clinical Research at Thermo Fisher Scientific at Thermo Fisher Scientific

Responsibilities

• Ensure protocol and regulatory compliance, manage documentation, and support clinical trials for leading pharmaceutical and biotech companies.

Employment details

• Location: Remote [India]

About the employer

• Learn more Equal Opportunity Policy Statement Thermo Fisher Scientific is an Equal Opportunity Employer.
• Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of more than $40 billion.
• Our Mission is to enable our customers to make the world healthier, cleaner and safer.
• Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them.
• Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD. www.thermofisher.com. --> Company About Us Suppliers Corporate Social Responsibility Information Security Investors Newsroom Careers Careers in Germany or Linz, Austria --> Brands Thermo Scientific Applied Biosystems Invitrogen Fisher Scientific Unity Lab Services Patheon PPD Connect For more information, please visit www.thermofisher.com Thermo Fisher Scientific is proud to be an equal opportunity employer.
• Qualified applicants will receive consideration for employment without regard to any characteristic protected by local, state, or federal laws, rules, or regulations. © 2024 Thermo Fisher Scientific, Inc.
• All Rights Reserved.
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Additional role details

• Seeking a Clinical Research Associate (Level II) to join our global team and coordinate all aspects of clinical monitoring and site management.
• Advance your career with impactful work in a dynamic, collaborative environment.
• expertise to the development of drugs that address the world’s most challenging health concerns.
• Our Clinical Research team, who powers our PPD® clinical research portfolio, are part of our leading global contract research organization (CRO).
• Accessibility/Disability Access We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment.
• Please contact us to request accommodation.
• All qualified applicants will receive consideration for employment without regard to any characteristic protected by local, state, or federal laws, rules, or regulations.
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