ICON plc

Clinical Trial Manager

ICON plc$90K — $120K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • BA/BS degree in health or science-related field
  • 2+ years of end-to-end trial management experience
  • Experience in early development multi therapeutic studies
  • Strong knowledge of ICH-GCP and local regulations
  • Proficient in relevant software; strong IT skills
  • Fluent in country language and English with effective communication skills
  • Legal authorization to work in the U.S. without sponsorship

Responsibilities

  • Manage central IRB and local vendor relations
  • Execute local study milestones from feasibility to close out
  • Coordinate country-level role resourcing and transitions
  • Maintain inspection readiness and AQR at the country level
  • Collaborate with Local Trial Managers and site teams to define responsibilities
  • Communicate efficiently with Clinical Trial Managers and support trial excellence
  • Lead ad hoc country-level meetings to address study challenges
  • Partner with study Functional Manager on updates, risks, and documentation

Benefits

  • Competitive base salary and performance-related incentives
  • Health and wellbeing programs including medical, dental, and vision coverage
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programs and wellbeing resources
  • Learning and development opportunities through structured training
Full Job Description
Local Trial Manager - Early Development Multi Therapeutic

The LTM for early development multi TA will manage and oversee the following throughout the study:
  • Central IRB and other local vendors (Greenphire, Drug Destruction services, etc....) including set up of vendor purchase orders, invoice review and approval, and change-orders, as applicable.
  • Execution of local milestones from feasibility through study close out.
  • Resourcing of country-level roles, including support with transitions, in collaboration and agreement with the study Functional Manager (FM).
  • Inspection Readiness and AQR at the country level.
  • Close collaboration with the assigned Local Trial Manager(s) (LTMs), Lead Site Manager (LSM), Site Managers (SMs), Clinical Trial Associates (CTAs), and Site Contract Managers (SCMs) to outline accountabilities/responsibilities and provide support and training, where necessary.
  • Efficient communication with the Clinical Trial Managers (CTMs), Clinical Operations and the Global Trial Leader (GTL) to oversee trial excellence.
  • Country level ad hoc meetings during any phase of the study that are needed to address unexpected circumstances that might impact country or study level deliverables.
  • Close partnership with the study FM to provide updates, discuss hurdles, timelines/resources, and potential risks, and assist with documentation, such as storyboards, lessons-learned, metrics, etc., that may be required by leadership.
  • Autonomy with execution of local trial management services
  • Depth of knowledge with local trial management services
  • Process leadership


What you need to have
  • BA/BS degree.
  • Degree in a health or science related field.
  • 2+ years of trial end to end management experience
  • Start-up & Database Locks/Cleaning experience preferred
  • Early Development multi therapeutic experience required
  • Strong working knowledge of ICH-GCP, company standard operating procedures, local laws and regulations, assigned protocols and associated protocol specific procedures.
  • Strong IT skills in appropriate software and company systems. Willingness to travel with occasional overnight stay away from home according to business needs.
  • Proficient in speaking and writing the country language and English. Good written and oral communication skills as appropriate
  • To qualify, applicants must be legally authorized to work in the United States and should not require, now or in the future, sponsorship for employment visa status


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.

About ICON plc

ICON plc is a global provider of drug development and commercialisation services to the pharmaceutical, biotechnology and medical device industries. The company specialises in the strategic development, management and analysis of programs that support clinical development. ICON has approximately 15700 employees in 40 countries. The company was founded in Dublin, Ireland in 1990 and is headquartered in Leopardstown, Dublin. ICON has been publicly traded on the NASDAQ since 1998.
Learn more about ICON plc
Size
39,300 employees
Market Cap
$16.2 billion
Industry
Net Income
$332.3 million
Founded
2017
5 Year Trend
+26.9%
Revenue
$2.7 billion
NASDAQ

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