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Study Start Up Associate I/Study Start Up Associate II

  1. Bangalore, Chennai, Bengaluru
JR127418
  1. Study Start Up
  2. ICON Full Service & Corporate Support
  3. Office Based

About the role

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Study Start Up Associate Level I & Level II

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

Study Start Up Associate.
As a member of the Study Start Up Team, you will play an integral role in making sure that physicians at our research sites are prepared to start the trial of investigational, new pharmaceutical and biological products for clinical trials at their local practices.

What you will be doing

  • Assisting in the preparation and submission of regulatory documents, such as clinical trial applications and ethics committee submissions.

  • Coordinating with internal and external stakeholders to obtain necessary approvals and authorizations for study initiation.

  • Maintaining accurate and up-to-date records of regulatory submissions and approvals.

  • Supporting study teams in the development of study documents, including protocols, informed consent forms, and investigator brochures.

  • Participating in study start-up meetings and providing input on regulatory requirements and timelines.

  • To review and negotiate clinical site investigator contracts and budgets.

  • Stay connected with Investigative sites, sponsors and internal personnel regarding the status of contracts and contract-related documents

  • Prepare and coordinate preparation of contractual documents and correspondence

  • Facilitate the indemnification process between the study sponsor and the site.

  • Function as the internal consultant on study budgets (investigator payments, develop and update training documentation and conduct group training as necessary, mentor and train new and junior personnel in the SSU department, and act as consultant on the Investigator Contract and Budget development process from origination through execution).


What you need:

  • Knowledge of ICH GCP and Prior clinical research experience with a minimum of 2-6 years’ experience in Essential Document review (Study Start Up)

  • Added Advantage:

    • Experience working with different countries

    • Proficiently review, negotiate and approve all Ethics Committee (EC), Institutional Review Board (IRB) and Competent Authority (CA) queries to Country and Site Specific ICFs.

#LI-AB2

What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs.
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply

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