ICON plc

Senior Clinical Trial Manager

ICON plc$100K — $130K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • BA/BS degree in a health or science related field.
  • 3 - 5+ years of trial end-to-end management experience.
  • Preferred experience in startup and database locks/cleaning.
  • Highly preferred background in immunology trial management.
  • Strong knowledge of ICH-GCP, local laws, and regulatory requirements.
  • Proficient IT skills and willingness to travel as needed.
  • Fluent in the country language and English with strong communication skills.

Responsibilities

  • Manage and oversee Central IRB and local vendors, including purchases and invoices.
  • Ensure execution of local milestones from feasibility to study closeout.
  • Oversee country-level roles and support transitions with Functional Manager.
  • Maintain inspection readiness and ensure adherence to quality standards.
  • Collaborate closely with LTMs, LSM, SMs, CTAs, and SCMs for accountabilities and training.
  • Facilitate efficient communication with CTMs and Global Trial Leaders for trial excellence.
  • Organize ad hoc meetings to address unexpected study issues.
  • Collaborate with study FM to discuss updates, risks, and documentation.

Benefits

  • Comprehensive health and wellbeing programmes including medical, dental, and vision coverage.
  • Retirement and pension plans available.
  • Life assurance and disability coverage offered.
  • Access to employee assistance programmes and wellbeing resources.
  • Opportunities for learning and career development through structured training.
Full Job Description
Senior Local Trial Manager - Immunology - Home Based (US)

The Sr LTM Immunology 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.
  • 3 - 5+ years of trial end to end management experience
  • Start-up & Database Locks/Cleaning experience preferred
  • Immunology trial management experience highly preferred
  • 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

Similar Jobs

More Jobs at ICON plc

More Pharmaceuticals & Biotech Jobs

Find similar Senior Clinical Trial Manager jobs: