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Position Name :

Scientific Affairs Specialist I

Organization :

Icon Plc

Qualification:

B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences

Experience:

1 to 2 Years

Salary:

Not disclosed

Location:

Bangalore

The Scientific Affairs Specialist I role at ICON plc in Bangalore is an exciting opportunity within a global healthcare intelligence and clinical research organization. Here’s a brief overview of the position:

Role Overview:

As a Scientific Affairs Specialist I, you will be involved in:

  • Collaborating with cross-functional teams to develop and review clinical trial protocols.
  • Analyzing clinical data to support decision-making and ensure trial integrity.
  • Providing scientific expertise to interpret study results and contribute to clinical trial reports.
  • Contributing to regulatory submissions by preparing scientific documents and responding to inquiries.
  • Keeping updated on scientific literature and industry developments to inform study design and strategy.

Candidate Profile:

  • Education: Bachelor’s degree in a scientific discipline; an advanced degree is preferred.
  • Experience: Prior experience in clinical research or the pharmaceutical industry.
  • Skills:
    • Strong analytical abilities and attention to detail.
    • Excellent written and verbal communication skills.
    • Ability to work both independently and collaboratively in a fast-paced environment.

Benefits:

ICON offers competitive benefits tailored to your country, which may include:

  • Various annual leave entitlements.
  • Health insurance offerings.
  • Competitive retirement planning options.
  • Access to the Global Employee Assistance Programme, LifeWorks.
  • Life assurance and flexible benefits like childcare vouchers, discounted gym memberships, etc.

Featured Courses

1

CLINI INDIA

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Courses:

  • Data Management
  • Pharmacovigilance
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  • Medical Coding
  • Regulatory Affairs
  • Clinical Research
2

CLINIVERSITY

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3

CLINIWINGS

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Coupon:

WINGS (10% Discount)

Courses:

  • Clinical Data Management
  • Pharmacovigilance
  • Medical Writing
  • Regulatory Affairs
  • Clinical Research