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Principal Scientific Communications / Clinical Scientist page is loaded
Principal Scientific Communications / Clinical Scientist
Apply
locations
United States - California - Santa Clara
time type
Full time
posted on
Posted 28 Days Ago
job requisition id
31087128
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.
JOB DESCRIPTION:
Principal Scientific Communications / Clinical Scientist 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. You’ll 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 bachelor’s 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 out of our Santa Clara, CA., location, and can also be based in the Minneapolis/St Paul area, in the Structural Heart (SH) Division. Our business purpose is to restore health and improve quality of life through the design and provision of device and management solutions for the treatment of structural heart disease. We have an exciting opportunity for the right candidate to join our rapidly growing clinical team within the SH division. The Scientific
Communications/Clinical
Scientist will be responsible for producing podium presentations, scientific publications, and clinical study reports for global regulatory submission using clinical data sets. The work will directly support evidence generation for transcatheter aortic valve implantation (TAVI) program. This position will work collaboratively with clinical scientists, biostatisticians, marketing, and other cross-functional leads. This position will also play a supporting role in interacting with clinical trial investigators to ensure the successful execution of clinical strategies to meet corporate podium and publication goals. What You'll Work On This position will work closely with cross-functional stakeholders in marketing, medical affairs, clinical affairs, biometrics, project management, data management, and other clinical groups. This position will also interact with physicians and regulatory authorities. Furthermore, this position will be required to execute the job responsibilities within the corporate policies and standard operating procedures. This position will: Responsible and accountable for execution of podium presentations, scientific publications, clinical study report writing for regulatory submission in collaboration with clinical program director and scientists
Ensure cross-functional alignment of prioritization of clinical evidence dissemination
Effectively communicate information through the planning and execution of meetings and presentations and present recommendations to all stakeholders
Ensure internal stakeholders are up to date on all activities supporting podium presentations (conference acceptances, presentation status) and publications status as well as clinical study report review
Drive internal and external collaborators to meet submission deadlines for conferences and journal submissions
Drive activities to meet the deadlines for internal approvals of clinical study reports for regulatory submissions
Oversee responses to journal reviewers and ensure they are handled in a timely manner
Ensure all data presented is cohesive and in alignment with Abbott standards
Support publication committee activities (planning and strategy) for key trials
Plays a key role in KOL management through strategic engagement while maintaining a collaborative relationship
Develops and maintains current, in-depth, relevant functional knowledge (such as scientific and technical aspects) of projects in support of the business on a global basis
Will perform this job in a quality system environment.
Prioritization across teams to ensure strategic goals/milestones within Clinical Affairs are met
Works with stakeholders to define business questions, requirements, timelines, objectives, and success criteria to address the need
Required Qualifications Bachelor's degree required; advanced degree preferred; degree in science, medicine, or a similar discipline is highly preferred.
Minimum of 8+ years of related work experience in clinical trials/medical writing
Cardiovascular and structural heart knowledge is a plus.
* Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free coverage applies in the next calendar year. Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:
www.abbottbenefits.com 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 www.abbott.com , on Facebook at
www.facebook.com/Abbott
and on X @AbbottNews. The base pay for this position is $109,300.00 – $218,500.00
In specific locations, the pay range may vary from the range posted. JOB FAMILY:
Clinical Affairs / Statistics
DIVISION:
SH Structural Heart
LOCATION:
United States > Santa Clara : Building A - SC
ADDITIONAL LOCATIONS:
United States > Minnesota > Plymouth : 5050 Nathan Lane N, United States > Minnesota > St. Paul > Tech Center : One St Jude Medical Drive
WORK SHIFT:
Standard
TRAVEL:
Not specified
MEDICAL SURVEILLANCE:
No
SIGNIFICANT WORK ACTIVITIES:
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday)Abbott is an Equal Opportunity Employer of
Minorities/Women/Individuals
with
Disabilities/Protected
Veterans.EEO is the Law link - English:
http://webstorage.abbott.com/common/External/EEO_English.pdf EEO is the Law link - Espanol:
http://webstorage.abbott.com/common/External/EEO_Spanish.pdf
#J-18808-Ljbffr
Principal Scientific Communications / Clinical Scientist
Apply
locations
United States - California - Santa Clara
time type
Full time
posted on
Posted 28 Days Ago
job requisition id
31087128
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.
JOB DESCRIPTION:
Principal Scientific Communications / Clinical Scientist 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. You’ll 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 bachelor’s 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 out of our Santa Clara, CA., location, and can also be based in the Minneapolis/St Paul area, in the Structural Heart (SH) Division. Our business purpose is to restore health and improve quality of life through the design and provision of device and management solutions for the treatment of structural heart disease. We have an exciting opportunity for the right candidate to join our rapidly growing clinical team within the SH division. The Scientific
Communications/Clinical
Scientist will be responsible for producing podium presentations, scientific publications, and clinical study reports for global regulatory submission using clinical data sets. The work will directly support evidence generation for transcatheter aortic valve implantation (TAVI) program. This position will work collaboratively with clinical scientists, biostatisticians, marketing, and other cross-functional leads. This position will also play a supporting role in interacting with clinical trial investigators to ensure the successful execution of clinical strategies to meet corporate podium and publication goals. What You'll Work On This position will work closely with cross-functional stakeholders in marketing, medical affairs, clinical affairs, biometrics, project management, data management, and other clinical groups. This position will also interact with physicians and regulatory authorities. Furthermore, this position will be required to execute the job responsibilities within the corporate policies and standard operating procedures. This position will: Responsible and accountable for execution of podium presentations, scientific publications, clinical study report writing for regulatory submission in collaboration with clinical program director and scientists
Ensure cross-functional alignment of prioritization of clinical evidence dissemination
Effectively communicate information through the planning and execution of meetings and presentations and present recommendations to all stakeholders
Ensure internal stakeholders are up to date on all activities supporting podium presentations (conference acceptances, presentation status) and publications status as well as clinical study report review
Drive internal and external collaborators to meet submission deadlines for conferences and journal submissions
Drive activities to meet the deadlines for internal approvals of clinical study reports for regulatory submissions
Oversee responses to journal reviewers and ensure they are handled in a timely manner
Ensure all data presented is cohesive and in alignment with Abbott standards
Support publication committee activities (planning and strategy) for key trials
Plays a key role in KOL management through strategic engagement while maintaining a collaborative relationship
Develops and maintains current, in-depth, relevant functional knowledge (such as scientific and technical aspects) of projects in support of the business on a global basis
Will perform this job in a quality system environment.
Prioritization across teams to ensure strategic goals/milestones within Clinical Affairs are met
Works with stakeholders to define business questions, requirements, timelines, objectives, and success criteria to address the need
Required Qualifications Bachelor's degree required; advanced degree preferred; degree in science, medicine, or a similar discipline is highly preferred.
Minimum of 8+ years of related work experience in clinical trials/medical writing
Cardiovascular and structural heart knowledge is a plus.
* Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free coverage applies in the next calendar year. Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:
www.abbottbenefits.com 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 www.abbott.com , on Facebook at
www.facebook.com/Abbott
and on X @AbbottNews. The base pay for this position is $109,300.00 – $218,500.00
In specific locations, the pay range may vary from the range posted. JOB FAMILY:
Clinical Affairs / Statistics
DIVISION:
SH Structural Heart
LOCATION:
United States > Santa Clara : Building A - SC
ADDITIONAL LOCATIONS:
United States > Minnesota > Plymouth : 5050 Nathan Lane N, United States > Minnesota > St. Paul > Tech Center : One St Jude Medical Drive
WORK SHIFT:
Standard
TRAVEL:
Not specified
MEDICAL SURVEILLANCE:
No
SIGNIFICANT WORK ACTIVITIES:
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday)Abbott is an Equal Opportunity Employer of
Minorities/Women/Individuals
with
Disabilities/Protected
Veterans.EEO is the Law link - English:
http://webstorage.abbott.com/common/External/EEO_English.pdf EEO is the Law link - Espanol:
http://webstorage.abbott.com/common/External/EEO_Spanish.pdf
#J-18808-Ljbffr