Ampcus, Inc
Senior Scientist Clinical Research
Ampcus, Inc, Titusville, New Jersey, us, 08560
Ampcus Inc. is a certified global provider of a broad range of Technology and Business consulting services. We are in search of a highly motivated candidate to join our talented Team.
Job Title:
Senior Scientist Clinical Research
Location(s):
Titusville, NJ
Job Responsibilities:
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 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 strategies 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.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.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 personnel, in preparation for health authority submissions.
Additional Clinical Research Responsibilities:
Partners with Regulatory Affairs in developing regulatory strategy and determining requirements for health authority reporting or corrective actions on trial/program level.May help explore and evaluate new assets (Client) and/or products to support compound value.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 the publication of clinical research findings. This may include presenting research results at internal/external meetings (i.e. investigator meetings and company sponsored events).
Qualification:
PhD in relevant field (e.g. Neuroscience, Biomedical Sciences, Biology; chemistry: pharmacy), PharmD or MD degree from an accredited institution with 1-2 years of work experience; or Masters in relevant field with 2-4 years of work experience.
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Job Title:
Senior Scientist Clinical Research
Location(s):
Titusville, NJ
Job Responsibilities:
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 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 strategies 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.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.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 personnel, in preparation for health authority submissions.
Additional Clinical Research Responsibilities:
Partners with Regulatory Affairs in developing regulatory strategy and determining requirements for health authority reporting or corrective actions on trial/program level.May help explore and evaluate new assets (Client) and/or products to support compound value.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 the publication of clinical research findings. This may include presenting research results at internal/external meetings (i.e. investigator meetings and company sponsored events).
Qualification:
PhD in relevant field (e.g. Neuroscience, Biomedical Sciences, Biology; chemistry: pharmacy), PharmD or MD degree from an accredited institution with 1-2 years of work experience; or Masters in relevant field with 2-4 years of work experience.
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