Senior Manager / Associate Director, Clinical Research Scientist

Incyte Corporation; New York, Wilmington (NY, DE); On-site; USD 90,000 - 150,000; Full time

Job summary

An established industry player in biopharmaceuticals seeks an Associate Director, Clinical Research Scientist to drive clinical programs. This pivotal role involves collaborating with physicians, developing protocols, and drafting essential scientific documents. The ideal candidate will bring a strong background in research and drug development, particularly in oncology. Join a forward-thinking company dedicated to improving patient lives through innovative medicines and impactful research. If you thrive in a fast-paced environment and possess excellent communication skills, this opportunity is perfect for you.

Qualifications

• Degree in a scientific or life sciences field; Pharm.D. or Ph.D. preferred.
• 2-4 years of research experience, with a minimum of 1 year in drug development.

Responsibilities

• Develop protocols for clinical studies and prepare clinical development plans.
• Draft clinical scientific documents and monitor safety and efficacy data.

Skills

Research experience

Drug development

Oncology knowledge

Communication skills

Analytical abilities

Education

Pharm.D. or Ph.D. in scientific or life sciences

Job description

Overview

Incyte is a biopharmaceutical company focused on the discovery, development, and commercialization of novel medicines to meet serious unmet medical needs in oncology and inflammation and autoimmunity. The company is committed to research and development excellence to improve patients' lives, impact healthcare positively, and build sustainable value.

Incyte aims to discover and develop first-in-class and best-in-class medicines, advancing a diverse portfolio of large and small molecules.

Job Summary (Primary Function)

The Associate Director, Clinical Research Scientist, is responsible for supporting clinical programs by collaborating with physicians within Clinical, based on assigned phases or therapeutic areas.

Essential Functions of the Job (Key Responsibilities)

• Develop protocols for clinical studies.
• Prepare clinical development plans.
• Draft clinical scientific documents such as INDs, amendments, Investigator Brochures, Annual Reports, and other FDA submissions.
• Monitor, review, and summarize safety and efficacy data from ongoing studies.
• Assist with study design for exploratory development.
• Lead clinical matrix teams for assigned compounds.
• Represent exploratory development on project teams.
• Build relationships with appropriate consultants.
• Write abstracts and present data at scientific meetings internally and externally.
• Serve as liaison to project teams, CROs, and other stakeholders.

Qualifications (Minimum Requirements)

• Degree in a scientific or life sciences field; Pharm.D. or Ph.D. preferred.
• At least 2-4 years of research experience, with a minimum of 1 year in drug development.
• Experience in oncology drug development is a plus.
• Ability to multitask and thrive in a fast-paced environment.
• Excellent written and oral communication skills.
• Strong analytical abilities.

Note: The above statements describe the general nature and level of work performed. They are not exhaustive, and duties may change as required.

Incyte is committed to diversity and is an equal opportunity employer.