Hiring.Camp

Study Start Up Associate I

Icon Plc

·

Today

Apply
Location
Argentina, Buenos Aires
Workplace
Remote
Type
Full-time
Seniority
Entry
Education
Bachelor
Source
Workday

Description

Study Start Up Associate I

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.


As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.


As a Study Start Up Associate I at ICON, you will facilitate the initiation of clinical trials, ensuring compliance with regulatory requirements, and contribute to the advancement of innovative treatments and therapies.


What You Will Do:

Your role will involve delivering site start-up and activation work to a high standard, working closely with your team and stakeholders.

Key responsibilities include:

  • 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.

Your Profile:

You will bring relevant site start-up and activation experience, along with the following qualifications and skills.

Required qualifications and experience:

  • Bachelor's degree in life sciences or a related field.
  • Previous experience in clinical research or regulatory affairs preferred, but Nt 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.
  • Advanced proficiency in English is required.

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

Skills

Clinical TrialsCompliance

Similar Jobs

30

Study Start Up Associate II

Icon Plc·São Paulo, Brazil·Remote

Today

Study Start Up Associate I

Icon Plc·Buenos Aires, Buenos Aires F.D.·Onsite

Today

Manager Study Start Up and Regulatory Affairs

Ergomed·Zagreb, Croatia·Remote

1d ago

Manager Study Start Up and Regulatory Affairs

Ergomed·Warsaw, Mazovia·Remote

1d ago

Manager Study Start Up and Regulatory Affairs

Ergomed·Belgrade, Central Serbia·Remote

1d ago

Manager Study Start Up and Regulatory Affairs

Ergomed·Sofia, Sofia-Capital·Remote

1d ago

Manager Study Start Up and Regulatory Affairs

Ergomed·Romania·Remote

1d ago

Manager Study Start Up and Regulatory Affairs

Ergomed·Prague, Czechia·Remote

1d ago

Manager Study Start Up and Regulatory Affairs

Ergomed·Rome, Lazio·Remote

1d ago

Manager Study Start Up and Regulatory Affairs

Ergomed·Portugal·Remote

1d ago

Manager Study Start Up and Regulatory Affairs

Ergomed·Madrid, Spain·Remote

1d ago

Manager Study Start Up and Regulatory Affairs

Ergomed·Guildford, England·Remote

1d ago

Study Start Up Associate II

Icon Plc·São Paulo, Brazil·Onsite

1d ago

Study Start Up Specialist Junior - Spain - FSP

Parexel·Spain·Remote

1d ago

Senior Study Start Up Associate

Icon Plc·Mexico City, Mexico +1·Onsite

1d ago

SSO Study Start-Up Manager

Novartis·Toranomon, Tokyo

2d ago

Country Study Start Up Specialist

AbbVie·Sydney, New South Wales·Hybrid

3d ago

Senior Specialist, Country Study Start Up

AbbVie·Sydney, New South Wales·Hybrid

3d ago

Site Contracts Negotiator - Study Start Up

Icon Plc·Barcelona, Catalonia +5·Onsite

3d ago

Study Start Up Manager - IQVIA Biotech - Portugal

Iqvia·Lisbon, Portugal

3d ago

Senior Study Start Up Associate

Icon Plc·Mexico City, Mexico·Onsite

6d ago

Study Start Up Specialist, Business Operations

Icon Plc·Sydney, New South Wales·Remote

6d ago

Regional Study Start Up Lead

Biibhr·Maidenhead, England·Hybrid

1w ago

Specialist, Country Study Start Up

AbbVie·Montréal, Quebec·Remote

1w ago

Research Study Start-Up Coordinator

Dartmouth Hitchcock·Lebanon, New Hampshire

1w ago

Senior Director, Global Study Start Up

AbbVie·New Jersey, US·Hybrid

1w ago

Copy of Senior Director, Global Study Start Up

AbbVie·South San Francisco, California·Hybrid

1w ago

Senior Director, Global Study Start Up

AbbVie·Irvine, California·Hybrid

1w ago

Senior Director, Global Study Start Up

AbbVie·North Chicago, Illinois·Hybrid

1w ago

Manager, Clinical Study Start-Up

Penumbra·Your Remote US Home Office·Remote

1w ago