Sr. Scientist Clinical Research
Sr. Scientist Clinical Research
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$ 86700 - 173300
1 Vacancy
Job Description
JOB DESCRIPTION:
Job Title
Sr. Scientist Clinical Research
About Abbott
Abbott is a global healthcare leader creating breakthrough science to improve peoples health. Were always looking towards the future anticipating changes in medical science and technology.
Working at Abbott
At Abbott you can do work that matters grow and learn care for yourself and family be your true self and live a full life. Youll also have access to:
- Career development with an international company where you can grow the career you dream of.
- Free medical coverage for employees* via the Health Investment Plan (HIP) PPO
- An excellent retirement savings plan with high employer contribution
- Tuition reimbursement the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelors degree.
- A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
- A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity working mothers female executives and scientists.
The Opportunity
This position works ONSITE in our Santa Clara CA (*Preferred) Temecula CA or New Brighton MN locations in the United States in the Abbott Vascular Division.
Abbott Vascular provides innovative minimally invasive and cost-effective products for treatment of vascular disease. Our extensive portfolio includes drug-eluting stents bare metal stents guide wires balloon dilatation catheters imaging catheters and software vessel closure devices and peripheral stents.
Interacts with various study support groups cross-functional teams in order to assist in clinical strategy the development of plans reports and project deliverables. Interacts with regulatory agencies as needed and will use their scientific and medical knowledge in order to provide directives to staff as well as study sites as directed by your manager.
What Youll Work On
- Writes clinical trial protocols protocol amendments clinical study reports and scientific publications. by evaluating scientific literatureanalyzingscientific data and staying abreast of current clinical practice.
- Facilitates regulatory submissions and communications by communicating with Regulatory Affairs during the submission process. Interacts with regulatory agencies as needed and will use scientific and medical knowledge to write strategic responses to questions from regulatory bodies about submissions.
- Participates in the development of clinical strategy and trial design by conducting meetings with the appropriate departments and individuals to obtain feedback/direction.
- Interacts with various study support groups cross-functional teams to assist in clinical strategy the development of plans reports and project deliverables. Is responsible for providing clinical feedback for other cross-functional deliverables.
- 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 RiskManagement Clinical Project Management external CROs or Medical Writers Training Senior Management and investigational sites as directed by your manager. Conducts team meetings drafting and sending routine correspondence (e.g. timelines meeting minutes) and/or by giving presentations to senior staff on project status.
- 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.
- Participates in and supports audits. May actively participate in root cause analysis. May participate in root cause analysis preventive or corrective actions and effectiveness monitoring.
- Understands business environment and relates extensive knowledge of internal and external technological activities to trends.
- Interfaces with senior management on significant matters often requiring the coordination of activity across organizational units.
- Responsible for compliance with applicable Corporate and Divisional Policies and procedures.
- Participates in the development of other technical contributors by facilitating training and providing feedback and guidance. May lead a project team.
- Provides technical leadership to business units physicians and oversees and directs external CROs and medical writers.
- 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. Erroneous decisions or recommendations would typicallyresult in failure to achieve major organizational objectives. Will perform this job in a quality system environment.
Required Qualifications
- Bachelors degree required; advanced degree preferred. Degree in the sciences medicine or similar discipline highly preferred.
- Minimum of 8years of related work experience with a complete understanding of specified functional area or an equivalent combination of education and work experience.
Preferred Qualifications
- Comprehensive knowledge of a technological field. Uses in-depth knowledge of business unit functions and cross group dependencies/ relationships.
- Is recognized as an expert in work group and across functions.
- Will perform this job in a quality system environment. Failure to adequately perform tasks can result in noncompliance with governmental regulations.
- Works on complex problems where analysis of situations or data requires an in-depth evaluation of various factors.
- Exercises judgment within broadly defined practices and policies in selecting methods techniques and evaluation criteria for obtaining results.
- Has broad knowledge of various technical alternatives and their potential impact on the business.
Please note that the salary range listed is our full grade range. We usually hire based on the mid-point.
Learn more about our health and wellness benefits which provide the security to help you and your family live full lives:
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer committed to employee diversity.
Connect with us at on Facebook at and on Twitter @AbbottNews and @AbbottGlobal.
The base pay for this position is
$86700.00 $173300.00In specific locations the pay range may vary from the range posted.
JOB FAMILY:
Clinical Affairs / Statistics
DIVISION:
AVD Vascular
LOCATION:
United States > Santa Clara : Building A - SC
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
Yes 5 % of the Time
MEDICAL SURVEILLANCE:
No
SIGNIFICANT WORK ACTIVITIES:
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day) Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day)Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
EEO is the Law link - English: EEO is the Law link - Espanol: Experience:
Senior IC
Employment Type
Full-Time
Key Skills
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