clinical scientist -first shift

$176,800 - $184,662/Yr

Randstad - Philadelphia, PA

Full-time - Mid Level

Remote - Philadelphia, PA

Administrative and Support Services

About the position

The Clinical Scientist role at Randstad US involves supporting the Clinical Development team in hematology/oncology drug development. The position focuses on formulating and executing the Global Development Plan (GDP) for assigned molecules and indications, ensuring data quality, and contributing to regulatory submissions. This role is primarily remote and requires a postgraduate degree, with responsibilities spanning data management, clinical study reporting, and cross-functional collaboration.

Responsibilities

• Review clinical study data; identify and evaluate study data trends, outliers, and protocol deviations; work with data management to issue and resolve queries to ensure data quality
• Contribute to clinical study reports, including reviewing and interpreting safety and efficacy data
• Participate in the cross-functional team meetings and address study or other program-specific questions
• Support execution and implementation of the Global Development Plan by providing strategic clinical science support for assigned studies and programs
• Contribute to or prepare clinical sections of relevant regulatory filings and meeting packages (INDs, meeting requests, NDAs, etc.)
• Work closely with other functional areas within R&D (clinical operations, data management, biostatistics, clinical pharmacology, nonclinical) to facilitate the execution of clinical trials and ensure high standards of study conduct are met
• Prepare clinical data and clinical program presentations
• Assist in reviewing and authoring study concept documents and clinical study protocols
• Write protocol summaries, process documents, investigator brochures, etc., in collaboration with cross-functional groups
• Provide input on clinical presentation slides for internal/external meetings and communications (e.g., investigator meetings, pre-study site selection visits, site training, study newsletters, communication to sites, etc.)
• Read and interpret scientific and medical literature for use in clinical documents and to assist clinical team decision-making

Requirements

• Excellent oral and written communication skills
• Proven ability to work independently and as part of a multidisciplinary team
• Collaborative and flexible in personal interactions with high emotional intelligence
• 2+ years of clinical/scientific research experience required, with solid tumor oncology expertise preferred
• 2+ years of experience working in a pharma/biotech company or postdoctoral or principal investigator experience within an academic or government setting
• PhD, MD, DO, PharmD, or other advanced scientific or clinical degree

Nice-to-haves

• Experience in hematology/oncology studies
• Familiarity with regulatory submissions and clinical trial processes

Benefits

• Health insurance
• 401K contribution
• Incentive and recognition program