Senior Clinical Scientist - single client dedicated

Remote Worker LTD.; United States; À distance; USD 140 000 - 200 000; Plein temps

Avantages offerts par ce poste

Competitive base salary

Health and wellbeing programmes

Retirement and pension plans

Life assurance and disability coverage

Employee assistance programmes

Career development opportunities

Résumé du poste

ICON is a global healthcare intelligence and clinical research organisation. We seek a Senior Clinical Scientist to design and conduct clinical studies evaluating safety and efficacy of innovative treatments.

You will lead cross-functional teams, author protocols and regulatory submissions, and drive clinical pharmacology initiatives across early programs.

Qualifications

• PhD, PharmD or MD, or 10+ years with BS/MS in early development/clinical pharmacology
• Ability to critically analyze problems and provide creative solutions
• Experience in clinical pharmacology, immunology or oncology is preferred
• Early phase/Phase I experience required

Responsabilités

• Provide strategic leadership for clinical programs supporting early development and clinical pharmacology
• Maintain knowledge of competitive landscape and act as SME on cross-functional teams
• Draft/review/approve protocols, analysis plans, study reports, and regulatory submissions with physicians and statisticians
• Execute Clinical & Clinical Pharmacology studies with Clinical Operations
• Review and summarize safety/efficacy data with the Medical Monitor
• Collaborate with Quantitative Clinical Pharmacology, Translational Sciences and Statistics on protocols and analyses
• Contribute to program strategy and clinical development plans
• Draft and review INDs, amendments, Investigator Brochures, Annual Reports and Health Authority submissions
• Ensure timelines and budgets are met for deliverables

Connaissances

Early phase experience

Clinical pharmacology

Immunology or oncology

Problem solving

Formation

PhD/MD/PharmD

BS/MS in related field

Description du poste

Senior Clinical Scientist

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

As a Senior Clinical Scientist at ICON, you will design and conduct clinical studies that evaluate the safety and efficacy of innovative treatments.

What You Will Do:

• Provide strategic leadership and demonstrating accountability for the clinical programs supporting early clinical development and clinical pharmacology

• Maintain updated knowledge of competitive landscape on current assets or evolving standards of care for indications of interest and provide subject matter expertise on cross-functional project teams

• Author/Review/Approve clinical protocols, analysis plans, study reports and regulatory submissions in collaboration with physicians, statisticians and other critical functions.

• Execute Clinical & Clinical Pharmacology studies in close collaboration with Clinical Operations

• Review and summarize clinical safety or efficacy data in collaboration with the Medical Monitor

• Work closely with Quantitative Clinical Pharmacology, Translational Sciences and Statistics to develop protocols and summarize analysis

• Contribute to the development of program strategy for assigned compounds/programs including participation in the preparation of clinical development plans

• Draft and review of clinical scientific documents such as IND, IND amendments, Investigator Brochures, Annual Reports and other Health Authority submissions

• Ensure adherence to agreed timelines and budgets to ensure prompt and accurate execution of deliverables from clinical studies and programs

Your Profile:

• At least 5 years’ experience and a, PhD, PharmD or MD degree or at least 10 years’ experience with BS/MS degree with emphasis on early development, clinical pharmacology or a related discipline

• Ability to critically analyze problems and provide creative solutions

• Experience in clinical pharmacology, immunology or oncology is preferred

• Early phase/Phase I experience required

#LI-REMOTE

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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.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.