Study Start Up Associate at ICON | Apply Now
A rare chance has emerged at ICON Strategic Solutions for the position of Study Start Up Associate I in Buenos Aires. This role involves facilitating the initiation of clinical trials and ensuring compliance with regulatory requirements, offering an opportunity to contribute to innovative treatments and therapies.
- Position: Study Start Up Associate I
- Location: Buenos Aires, Argentina – Remote
- Job ID: JR160878
About ICON Strategic Solutions
ICON Strategic Solutions is a leading global provider of outsourced development and commercialization services to the pharmaceutical, biotechnology, and medical device industries. As part of the world’s largest FSP organization, ICON operates with over 90 sponsor partnerships, delivering stability, career development, and a collaborative environment that supports the advancement of treatments benefiting patients worldwide.
Job Description
As a Study Start Up Associate I at ICON, the successful candidate will facilitate the initiation of clinical trials, ensuring compliance with regulatory requirements. This role is pivotal in contributing to the advancement of innovative treatments and therapies while working closely with teams and stakeholders to deliver high-quality site start-up and activation work.
Eligibility Criteria
The ideal candidate will possess relevant site start-up and activation experience, along with the following qualifications:
- Bachelor’s degree in life sciences or a related field.
- Previous experience in clinical research or regulatory affairs preferred, but not required.
- Strong attention to detail and organizational skills.
- Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams.
- Ability to work independently and manage multiple tasks simultaneously in a fast-paced environment.
Study Start Up Associate Responsibilities
- 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.
The opportunity at ICON Strategic Solutions for the role of Study Start Up Associate I is an excellent chance for qualified individuals to contribute to the clinical research field. Interested candidates should apply before the deadline to seize this opportunity.
