Abbott · 1 day ago
Senior Clinical Research Scientist
Abbott is a global healthcare leader that helps people live more fully at all stages of life. The Senior Clinical Research Scientist will provide scientific expertise throughout the development and implementation of clinical evaluations and studies, interacting with various teams to assist in clinical strategy and project deliverables.
BiotechnologyEmergency MedicineGeneticsHealth CareHealth DiagnosticsManufacturingMedicalMedical DeviceNutritionPharmaceutical
Responsibilities
Writes clinical evaluation plans and reports, study protocols, protocol amendments, informed consents, study reports, risk master lists, and scientific papers for publication by evaluating scientific literature, analyzing scientific data and staying abreast of current clinical practice
Examine data sets and determine the best end-to-end analysis plan to address key scientific questions
Analyzes data (including defining populations, creating model logic, drawing insights, refining analyses and determining outcomes
Present analysis results in a cohesive manner
Interprets results in preparation for product applications by evaluating clinical and scientific and risk data and literature, and staying abreast of current clinical practice
Presents scientific data by communicating accurate, succinct summaries of clinical results at industry gatherings, investigational meetings, and regulatory agency meetings
Facilitates communication between Sales and Marketing, R&D, Clinical R&D, Regulatory Affairs, Library Services, Product Performance Group (PPG), Quality Engineering, Clinical Affairs or Clinical Science, Risk Management, Clinical Project Management, external CROs or Medical Writers, Training, Senior Management and investigational sites as directed by your manager
Participates in the development of clinical strategy and trial design by conducting meetings with the appropriate departments and individuals to obtain feedback/direction
Creates, manages, or participates in clinical study or clinical evaluation timelines and budgets by utilizing the appropriate project management tools, selecting providers or external medical writers, managing vendor contracts as requested, and ensuring expenditures are within budgetary guidelines
Facilitates regulatory submissions and communications by communicating with Regulatory Affairs during the submission process
Participates in and supports audits
Interfaces with management on significant matters, often requiring the coordination of activity across organizational units, physicians, and external CROs and medical writers
Participates in the development of other technical contributors by supporting training and providing feedback and guidance
Conducts team meetings, drafting and sending routine correspondence and presenting regular updates to senior staff
May participate in a project team, root cause analysis, preventive or corrective actions, and effectiveness monitoring
Acts as a mentor to less-experienced staff and may provide work direction or supervise other technical employees
Exercises judgment independently
Plans and organizes project assignments of substantial variety and complexity
Qualification
Required
Bachelor's degree in science or engineering, or related discipline
Minimum 5 years related work experience or an equivalent combination of education and work experience
Preferred
Advanced Degree (PhD, MD, etc) + 2 years relevant work experience
Strong independent data analysis and programming skills (R, SPSS, SAS, MatLab, etc.)
Strong Data Communication and Figure Creation Experience
Understanding of statistical principles
Benefits
Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
An excellent retirement savings plan with a high employer contribution.
Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.
Company
Abbott
Abbott is a healthcare company that produces diagnostic kits, medical devices, nutritional products, and branded generic medicines.
Funding
Current Stage
Public CompanyTotal Funding
$6.79M2011-03-15Post Ipo Debt· $0.1M
2009-03-16Post Ipo Debt· $6.69M
1980-12-12IPO
Recent News
2026-01-07
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