ICON plc

Global Trial Optimization Specialist

ICON plc • $100K — $120K *
US-AnywhereRemote in Blue Bell, PA
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree in medicine, pharmacy, nursing, or biological science
  • 3+ years clinical trial experience, with 2 years preferred in a relevant analytics role
  • Experience in pharma or CRO environments preferred
  • Feasibility experience required
  • Oncology clinical research background required
  • Proven analytical and data synthesis skills
  • Strong presentation abilities

Responsibilities

  • Develop patient recruitment and retention strategies for clinical trials
  • Consult on recruitment and retention for ongoing projects
  • Manage project scope, deliverables, and timelines
  • Serve as the main point of contact for client communications
  • Select and oversee recruitment and retention vendors
  • Coordinate project activities to ensure milestone adherence
  • Stay updated on recruitment trends and technologies

Benefits

  • Health and wellbeing programs including medical, dental, and vision
  • 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
Global Trial Optimization Specialist - Oncology - Home Based (US)
At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise.

What will you be doing?
  • Develop strategic patient recruitment and retention recommendations to aid clinical trial teams to execute clinical studies within proposed timelines
  • Serve as expert consultant to project teams for existing projects needing recruitment and retention support
  • Manage the scope of work, objectives, quality of deliverables, and other activities of assigned projects (based on scope, may co-manage or independently manage these projects)
  • Serve as primary project contact for Patient Recruitment and Retention programs with sponsor to maintain appropriate communication channels and adherence to reporting schedules as required
  • Select and manage recruitment and retention vendors
  • Coordinate strategy-related project activities for study team and sponsor to confirm that overall project milestones are met
  • Maintain knowledge of current and innovative recruitment trends, vendors, and technologies to increase productivity and recommend additional support as needed
  • Leverage internal and external intelligence to support and refine strategies on assigned projects
  • Support continued process improvement to maintain quality within the organization


What you need to have:

Education: Bachelor's Degree, preferably in a medicine, pharmacy, nursing or biological science

Experience:
  • At least 3 years of career experience including 2 years in the conduct of clinical trials and some knowledge in business process analytics and continuous improvement highly preferred
  • Pharma and/or CRO experience highly preferred
  • Feasibility Experience required
  • Patient recruitment strategy planning experience (at site and country level)
  • Oncology clinical research background experience required
  • Analytical skills and ability to synthesize data
  • Excellent presentation skills
  • Ability to work well in a fast-paced environment

Skills:
  • Robust analytical skills and ability to synthesize data and differing points of view to navigate to an evidence-based data-driven solution
  • Ability to negotiate and influence stakeholders.
  • Strong interpersonal and communication skills
  • Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines
  • Superior presentation skills
  • Demonstrated ability to identify risks to execution and contribute to planned solutions
  • Computer skills including proficiency in aspects of data analysis and presentation software, Microsoft Word, and Excel
  • Excellent organizational and problem solving skills
  • Effective time management skills and ability to manage competing priorities
  • Ability to establish and maintain effective working relationships in a matrix environment
  • Travel of 10% could be expected for client meetings and Investigator Meetings. IMs could be domestic or international travel.
  • 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.

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

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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