Mindblowing Jobs

Clinical Study Manager II

By Admin · Clinical Research & Clinical Operations

BANGALORE (IN)HYBRIDPOSTED: 9/24/2026
PHARMAFull-time
HIRING ORGANIZATIONICONContract Research Organization (CRO) / Clinical Research / Healthcare Services
ICON

ROLE OVERVIEW

Manage day-to-day clinical trial activities and lead planning, execution, monitoring, and issue resolution for complex clinical studies. The role supports sponsor-dedicated clinical development programmes while ensuring regulatory compliance, data integrity, quality, timelines, and efficient resource utilization.

ROLE DEFINITION & RESPONSIBILITIES

  • •Bachelor's degree in a relevant scientific discipline or healthcare-related field
  • •Extensive clinical study management experience
  • •Good understanding of the drug development process and regulatory landscape
  • •Proven project management and prioritization skills
  • •Strong communication and interpersonal skills
  • •High attention to detail and commitment to data accuracy and quality
Reporting Hierarchy: ICON is a global clinical research organization and FSP provider supporting pharmaceutical and biotechnology companies in the development of medicines and therapies. ICON Strategic Solutions operates through sponsor-dedicated partnerships and global clinical-development expertise.

* Role responsibilities and qualifications synthesized based on industry benchmark standards.

QUALIFICATIONS & REQUIREMENTS

REQUIRED QUALIFICATIONS

  • Experience managing complex or advanced clinical trials
  • Sponsor-dedicated or FSP experience
  • Experience managing investigators and vendors
  • Experience with study budgets, timelines, and resource planning
  • Experience developing or mentoring clinical study teams

PREFERRED QUALIFICATIONS

  • •Reports within ICON Strategic Solutions and works in a sponsor-dedicated model
  • •Collaborates with investigators, vendors, internal cross-functional teams, and sponsor stakeholders

REQUIRED VERIFIED SKILLS

Sponsor-dedicated clinical research
FSP operations
team development
resource optimization
clinical study planning
cross-functional collaboration
strategic problem solving

COMPENSATION & REWARDS

Salary: Competitive / Disclosed upon candidate shortlisting
Bonus & Equity: Competitive base salary and performance related incentives
Benefits: Health and wellbeing programmes including medical, dental and vision coverage where applicable; retirement and pension plans; life assurance and disability coverage; employee assistance programmes; learning and development opportunities
Highlight extensive clinical study management experience and relevant scientific or healthcare education; demonstrate experience leading complex clinical trials from planning through execution and monitoring; quantify responsibility for budgets, timelines, vendors, investigators, and study teams; emphasize regulatory knowledge, data integrity, quality management, and issue resolution; showcase cross-functional communication and prioritization skills.

ORGANIZATION CONTEXT & CULTURE

Contract Research Organization / Clinical Research

TEAM SIZE: ICON emphasizes collaborative working, career development, inclusion, accessibility, patient impact, and sponsor-dedicated clinical research delivery.
INDUSTRY: Contract Research Organization (CRO) / Clinical Research / Healthcare Services
Culture: 2026-09-25

EXPECTED CAREER ROADMAP

The posting states that ICON offers a competitive base salary and performance-related incentives but does not disclose specific salary amounts. Benefits and compensation may vary by role and location.

APPLICATION ADVISORY

[https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Clinical-Study-Manager-II_JR156284/apply?locationCountry=c4f78be1a8f14da0ab49ce1162348a5e
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