New 
Clinical Research Scientist - III
 Spectraforce Technologies | |
 United States, New Jersey, Avenel | |
 Aug 10, 2026 | |
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Job Title: Clinical Research Scientist - III
Duration: Potential for conversion following 12 months depending on needs of the business Location: Remote Schedule is flexible but generally 9:00-17:00, can support EST or PST, remote Description: * Acquires and utilizes knowledge of clinical trial design to develop specific study concept sheets and protocols. * Participates in protocol review discussions concerning scientific and procedural aspects of study design. * Prepares study protocols, amendments, specific sections of study manuals and Investigator meeting notebooks, and other documents as needed with appropriate guidance and supervision. * With supervision, contributes to the design and development of CRFs, Data Management Manuals and Data Analysis Plans. * With supervision, addresses questions regarding scientific and related procedural issues from Investigators. * With supervision, contributes to the preparation and/or review of data listings, summary tables, study results, manuscripts, and scientific presentations. * Assists in the preparation/review of regulatory documents, IND annual reports, IND safety reports, Investigator Brochures and NDAs. * Supports priorities within functional area. Anticipates moderately complex obstacles within a clinical study and with guidance implements solutions. * May be asked to coordinate teams and provide direction. * May lead two or more specific components of departmental strategic initiatives. * Must be able to enter a new therapeutic area and summarize scientific information that is available in published literature to integrate into new study development. * Excellent verbal and written communication skills and interpersonal skills are required to maintain working relationship with team members to ensure scientific integrity of clinical studies. * May be sought out for advice by others within the company to help make better decisions and resolve moderately complex problems. Requirements: PharmD with 2+ years relevant scientific and/or drug development experience MS with 6+ years' relevant scientific and/or drug development experience. BS or RN with 8+ years' relevant scientific and/or drug development experience | |