Clinical Scientist
2 months ago
Source One Technical Solutions is seeking a Clinical Scientist for an exciting hybrid (mostly remote) consulting opportunity with a global pharmaceutical company based in Mercer County, NJ.
No sponsorships or C2C
Job Title Clinical Scientist (Contractor)
The contract duration is initially 6-12 months, with a likely extension
40 hours/week, Mon-Fri
Description:
Responsible for the translation and implementation of (non-medical) scientific concepts into the study design and/or program across planning, execution, and reporting, including integration of biomarkers, digital technologies, data science initiatives, and select vendors
Job Responsibilities:
- Program/Trial Planning, Execution and Reporting
- Responsible for leading the translation of scientific concepts into program and study design
- Responsible for identifying and implementing (non-medical) scientific aspects of the program and/or study at planning, execution and reporting, including (but not limited to) integration of Biomarkers and Data Science/Digital Health initiatives into studies.
- Oversees the assessment, selection and operational implementation for biomarkers, digital and other endpoints (scales), imaging
- Accountable for shaping and implementing compound and program DEI strategy together with Clinical Leader
- Provides expert input in clinical development plans
- Contributes to the preparation of PED, study protocols and training materials for clinical studies.
- Prepares for and participates in Protocol review Committee (PRC) and First in Human (FIH) Committee meetings
- Reviews medical and scientific literature
- Along with SRP or Clinical Leader and global development partners, responsible for oversight and high-quality implementation and closure of the study, ensuring data integrity
- Responsible for the TA review and sign off on various operational plans
- Responsible for scientific input into HA and EC responses.
- In concert with operational staff, acts as a liaison between the company and clinical investigators for overarching scientific guidance and other potential non-medical aspects
- Works closely with Data Sciences, Data Management, Statistics, Programming, JJIT and others to ensure data are received in the manner needed to support trial outcomes
- Responsible for the review of the data to ensure quality and to identify data quality trends.
- Sets up and leads Adjudication Activities
- Leads data visualization (DV) meetings and ensures decisions are documented and communicated internally and externally
- Owns contracting with clinical consultants, IDMC members and KOLs, including payment oversight.
- Participates in vendor oversight focusing on the integration of data and technology in clinical trials
- Contributes to completion of clinical study reports
- Contributes to the interpretation, reporting and preparation of oral and written results of product research in concert with senior clinical personal, in preparation for health authority submissions.
Additional Clinical Research Responsibilities:
- Partners with Regulatory Affairs in developing regulatory strategy and determining requirement for health authority reporting or corrective actions on trial/program level
- May help explore and evaluate new assets (BD) and/or products to support compound value
- Safety Management
- Oversees the set-up of medical review tools to meet medical review plan requirements
- Participates in Data Review Meetings
- Qualified CS may perform aspects of medical review under supervision of CL or SRP
- Safety monitoring summaries linked to quarterly medical reviews and/or monthly medical reviews may be delegated to qualified CS
- Assists in organizing content for IDMC presentation
- External Communication and Publication
- Contributes in all areas where scientific data will be generated and shared with the patients and/or the scientific community
- May be asked to assess medical publications emerging from the Team and its affiliates
- May act, in concert with senior clinical personnel, as the company spokesperson regarding publication of clinical research findings. This may include presenting research results at internal/external meetings (i.e. investigator meetings and company sponsored events)
Notes from the hiring manager on this role:
- Can be Hybrid, but is moving this to more Remote
- Should be in EST time zone
- Should be local to work site, it could go to hybrid (1 day onsite)
- This group supports the Clinical Team (Neuroscience), currently conducting an MG Study
- Must have a Bachelor's Degree, in Neuroscience would be great
- Must have Clinical Scientist experience
- Must have at least 3-5 years of experience
- Will be responsible for Translation & Implementation of Scientific Concepts (Non-Medical)
- Experience with Planning, Execution, and Reporting
- Integration of Biomakers & Data Science
- No Lab experience required
- Must have experience in Pharma or Clinical
Top Skills:
- Data Review exp
- Study Close Out exp
- Clinical Scientist exp
- Data Monitoring exp
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