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Kaztronix
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Clinical Research Scientist Early Development
We are seeking a motivated Clinical Research Scientist to join our Clinical Development team and support the execution of innovative clinical studies. This individual will work closely with senior scientists, physicians, and cross-functional partners to contribute scientific expertise, data insights, and clinical input across multiple programs.
Key Responsibilities
Qualifications
Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.
By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.
Clinical Research Scientist
Iselin, NJ US
Job Description
Clinical Research Scientist Early Development
We are seeking a motivated Clinical Research Scientist to join our Clinical Development team and support the execution of innovative clinical studies. This individual will work closely with senior scientists, physicians, and cross-functional partners to contribute scientific expertise, data insights, and clinical input across multiple programs.
Key Responsibilities
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Assist in the design and development of study protocols and protocol amendments.
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Contribute to the preparation of clinical and regulatory documents, including sections of INDs, study reports, investigator brochures, and updates for health authorities.
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Provide scientific input into study tools such as case report forms, statistical analysis plans, and data output specifications.
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Participate in the review and interpretation of clinical safety and efficacy data;support data monitoring activities throughout study conduct.
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Collaborate with internal study teams and external partners (CROs, vendors, investigators) to ensure high-quality study execution.
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Present study progress and scientific updates to project leadership and cross-functional committees.
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Support preparation of data for abstracts, posters, presentations, and manuscripts.
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Stay informed on evolving therapeutic landscapes, competitive intelligence, and standards of care relevant to assigned programs.
Qualifications
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Advanced degree in a life science discipline preferred (Pharm.D., Ph.D., or equivalent).
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1 3 years of experience in clinical research, with at least 1 year in drug development or industry setting.
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Background in oncology or hematology is a plus.
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Strong analytical skills and attention to detail, with ability to interpret and communicate complex data.
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Excellent organizational, written, and verbal communication skills.
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Ability to work effectively in a fast-paced, collaborative environment and manage multiple priorities.
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Willingness to travel occasionally (up to ~20%).
Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.
By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.
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