10,622 Clinical Scientist jobs in the United States

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
**Working at Abbott**
At Abbott, you can do work that matters, grow, and learn, care for yourself and your 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.
+ 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.
+ A company recognized as a great place to work in dozens of countries worldwide 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 the best place to work for diversity, working mothers, female executives, and scientists.
**The Opportunity**
This position works out of our Alameda, CA location in the Diabetes Care division where we're focused on helping people with diabetes manage their health with life-changing products that provide accurate data to drive better-informed decisions. We're revolutionizing the way people monitor their glucose levels with our new sensing technology.
The Clinical Scientist II serves as subject matter expert to build and improve the scientific presence in the marketplace and support the marketing strategies on a worldwide basis by providing technical expertise. Helps protect or promote sales of products by reviewing contents for Clinical/Medical and Scientific Affairs functions to ensure claims are substantiated appropriately and consistent with medical terminology and practice.
**What You'll Work On**
-Review Ad-Promo content for Clinical and Scientific Affairs function. Provides clinical/technical support to Scientific and Medical Affairs to address product related queries.
-Generate literature summaries and technical write-ups for regulatory submissions .
-Support writing papers and presentations for publication in peer-reviewed medical and/or scientific journal of conferences.
-Interfaces with key stakeholders on tasks (e.g., Regulatory, R&D, Quality, Marketing, Medical Affairs).
-Creates/updates technical documents for medium risk product international regulatory submissions (e.g., IVDR Class C/D and/or novel).
-Creates/updates technical documents for medium risk product domestic regulatory submissions (e.g., Class III and/or de novo).
-Prepares associated product labeling and clinical labeling (vial, kit labels), instructions for use and clinical brochures for high risk/high visibility products (e.g., IVDR Class C/D or US Class III, novel products, de novo products).
-Completes templated or untemplated verification and stability records for high risk/high visibility products.
-Creates and updates troubleshooting guides.
-Coordinates all activities related to the tasks above by locating inputs for documents, navigating systems related to international and domestic regulatory submission, labeling, records, and troubleshooting guides; utilizing, proposing, and making updates to templates, tools, and best practices for assigned tasks; and independently scheduling and running cross-functional team meetings.
-Seeks out solutions and resolves issues independently on tasks, projects, and in cross-functional team meetings.
**Required Qualifications**
- Bachelor's degree in science (biology, chemistry, microbiology, immunology, medical technology, pharmacy, pharmacology), math, engineering, or medical fields is preferred.
- Equivalent Combination of Education and Experience in lieu of a degree.
- 5 years' Experience in Medical Writing or a related field
Apply Now ( base pay for this position is $86,700.00 - $173,300.00. In specific locations, the pay range may vary from the range posted.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email

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 Title**
**Principal 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 of which you dream.
+ 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 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 may work out of any of our Vascular Division sites: Santa Clara, CA, Temecula, CA, St. Paul, MN, Westford, MA. Abbott Vascular provides innovative, minimally invasive, and cost-effective products for the treatment of vascular disease. **THIS IS AN ONSITE DAILY REQUIRED POSITION.**
**_MAIN RESPONSIBILITIES_**
+ Design clinical trials and studies in collaboration with internal stake holders including clinical project management, clinical operations, biostatistics, data management, regulatory affairs, medical affairs as well as external stake holders including steering committees, and national principal investigators to support device premarket approval (PMA) applications and premarket notification submissions (510(k)) to the FDA, and strategic business needs.
+ Provide scientific and technical direction and feedback. Provide scientific leadership to Cross Functional and Marketing/Commercial Teams to support business priorities and serve as Clinical Science lead on study teams and provide scientific support to justify trial design and ongoing scientific analysis during protocol development. May include generation of pre-protocol documentation of scientific information, including pre-submissions to FDA.
+ Lead the generation of study-related documents and/or contribute content and oversight of such documents, including, clinical study protocols, case report forms, clinical study reports, and informed consent forms.
+ Critically analyze data and present to internal and external groups including but not limited to clinicians and cross-functional team members.
+ Develop the scientific podium and publication strategy in close collaboration with cross-functional teams and lead the execution of the publication strategy.
+ Lead/collaborate on submission of abstracts, presentations, and publications of clinical study data, working with investigator authors and internal teams.
+ Synthesize literature and competitive information across multiple products and/or therapies within the assigned therapeutic area.
+ Review and critically assess statistical analysis plans.
+ Generate documents to support regulatory submissions for Abbott products and/or respond to questions from regulatory authorities about existing submissions.
+ Attend, present at, and lead meetings with FDA and other regulatory bodies.
+ Contribute to the optimization of internal processes and workflows.
+ Develop new ideas for both external and internal projects.
+ Mentor junior team members.
+ Perform other related duties and responsibilities, on occasion, as assigned.
**EDUCATION AND EXPERIENCE YOU'LL BRING:**
**Required Qualifications**
+ Bachelor's degree required, advanced degree preferred. Degree in the sciences, medicine, or similar discipline highly preferred.
+ Minimum of 8+ years of related work experience with a complete understanding of specified functional area, or an equivalent combination of education and work experience.
+ Comprehensive knowledge of a particular technological field.
+ Uses in-depth knowledge of business unit functions and cross group dependencies/ relationships
+ 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.
**Preferred Qualifications**
+ MS Office Suite, highly preferred
+ Experience in the medical device industry, highly preferred
+ Experience with clinical trials, highly desirable
+ Experience in a vascular/cardiovascular fields, a plus
Please note that the salary range listed is our full grade range. We usually hire based on the mid-point.
Apply Now ( more about our health and wellness benefits, which provide the security to help you and your family live full lives:** ( 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 $112,000.00 - $224,000.00. In specific locations, the pay range may vary from the range posted.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email

**Duration: 6 months contract**
**Job Description:**
**Onsite or remote:** Location **strongly prefer Boston / Waltham** -to enable partnership with the TA MD. If remote has to be in tied with Client Hub - **Chicago (2nd preference)** or **South San Francisco (3rd preference).**
+ Contribute to the **review, interpretation and communication of scientific data** pertaining to the efficacy and safety of compounds in development. Attends **congress and reviews literature** to develop and augment expertise in **therapeutic area**
+ Help develop program strategy including the **clinical development plan, product lifecycle plans, target product profiles and draft labels.** Reviews competitive landscape and help identify and evaluate business development opportunities.
+ Responsible for providing focused scientific and clinical study support from **start-up clinical study report (CSR).**
+ Participate in **scientific education of internal and external stakeholders** on the **pre-clinical (e.g. mechanism of action, animal models)** and clinical **(e.g. epidemiology, diagnosis, treatment)** data relevant to program. Engage opinion leader interactions to build pipeline awareness and foster research collaborations.
+ Contribute to the **scientific content of Study Protocols, Investigator Brochures, Clinical Study Reports, Informed Consent Forms, briefing documents, charters, and regulatory documents.**
+ Contribute to **creation of electronic database, IRT,** and associated training documents and review data completeness and fidelity throughout study conduct.
+ Collaborate cross-functionally to help create a scientific platform in support of the regulatory, commercial and medical education strategy for late-stage assets.
+ Ensure adherence to **Good Clinical Practices, pharmacovigilance standards, standard operating procedures** and to all other quality standards in conducting research. Contributes to authorship of regulatory responses and may participate in meetings.
**Responsibilities:**
+ Contribute to the **review, interpretation and communication of scientific data** pertaining to the efficacy and safety of compounds in development. Attends **congress and reviews literature** to develop and augment expertise in **therapeutic area**
+ Help develop program strategy including the **clinical development plan, product lifecycle plans, target product profiles and draft labels.** Reviews competitive landscape and help identify and evaluate business development opportunities.
+ Responsible for providing focused scientific and clinical study support from **start-up clinical study report (CSR).**
+ Participate in **scientific education of internal and external stakeholders** on the **pre-clinical (e.g. mechanism of action, animal models)** and clinical **(e.g. epidemiology, diagnosis, treatment)** data relevant to program. Engage opinion leader interactions to build pipeline awareness and foster research collaborations.
+ Contribute to the **scientific content of Study Protocols, Investigator Brochures, Clinical Study Reports, Informed Consent Forms, briefing documents, charters, and regulatory documents.**
+ Contribute to **creation of electronic database, IRT,** and associated training documents and review data completeness and fidelity throughout study conduct.
**Experience:**
+ **Experience Level = 3-5 Years**
+ **Oncology clinical trial experience** in the **Oncology (preferably solid tumors)** therapeutic area in the pharmaceutical industry
+ **Hands on experience** with **data review and clean, data analysis with extensive experience using EDC, CTMS and other database.**
+ Knowledge of **clinical trial methodology, regulatory and compliance requirements governing clinical trials and experience in the design of study protocols**
**Skills:**
+ **Oncology clinical trial experience** in the **Oncology (preferably solid tumors)** therapeutic area in the pharmaceutical industry
+ **Hands on experience** with **data review and clean, data analysis with extensive experience using EDC, CTMS and other database.**
+ Contribute to the **scientific content of Study Protocols, Investigator Brochures, Clinical Study Reports, Informed Consent Forms, briefing documents, charters, and regulatory documents.**
**Education:**
+ **Bachelors degree** in the sciences; advanced degree **(e.g., MS, PhD, PharmD)** preferred.
**About US Tech Solutions:**
US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

**Duration: 6 months contract**
**Job Description:**
**Onsite or remote:** Location **strongly prefer Boston / Waltham** -to enable partnership with the TA MD. If remote has to be in tied with Client Hub - **Chicago (2nd preference)** or **South San Francisco (3rd preference).**
+ Contribute to the **review, interpretation and communication of scientific data** pertaining to the efficacy and safety of compounds in development. Attends **congress and reviews literature** to develop and augment expertise in **therapeutic area**
+ Help develop program strategy including the **clinical development plan, product lifecycle plans, target product profiles and draft labels.** Reviews competitive landscape and help identify and evaluate business development opportunities.
+ Responsible for providing focused scientific and clinical study support from **start-up clinical study report (CSR).**
+ Participate in **scientific education of internal and external stakeholders** on the **pre-clinical (e.g. mechanism of action, animal models)** and clinical **(e.g. epidemiology, diagnosis, treatment)** data relevant to program. Engage opinion leader interactions to build pipeline awareness and foster research collaborations.
+ Contribute to the **scientific content of Study Protocols, Investigator Brochures, Clinical Study Reports, Informed Consent Forms, briefing documents, charters, and regulatory documents.**
+ Contribute to **creation of electronic database, IRT,** and associated training documents and review data completeness and fidelity throughout study conduct.
+ Collaborate cross-functionally to help create a scientific platform in support of the regulatory, commercial and medical education strategy for late-stage assets.
+ Ensure adherence to **Good Clinical Practices, pharmacovigilance standards, standard operating procedures** and to all other quality standards in conducting research. Contributes to authorship of regulatory responses and may participate in meetings.
**Responsibilities:**
+ Contribute to the **review, interpretation and communication of scientific data** pertaining to the efficacy and safety of compounds in development. Attends **congress and reviews literature** to develop and augment expertise in **therapeutic area**
+ Help develop program strategy including the **clinical development plan, product lifecycle plans, target product profiles and draft labels.** Reviews competitive landscape and help identify and evaluate business development opportunities.
+ Responsible for providing focused scientific and clinical study support from **start-up clinical study report (CSR).**
+ Participate in **scientific education of internal and external stakeholders** on the **pre-clinical (e.g. mechanism of action, animal models)** and clinical **(e.g. epidemiology, diagnosis, treatment)** data relevant to program. Engage opinion leader interactions to build pipeline awareness and foster research collaborations.
+ Contribute to the **scientific content of Study Protocols, Investigator Brochures, Clinical Study Reports, Informed Consent Forms, briefing documents, charters, and regulatory documents.**
+ Contribute to **creation of electronic database, IRT,** and associated training documents and review data completeness and fidelity throughout study conduct.
**Experience:**
+ **Experience Level = 3-5 Years**
+ **Oncology clinical trial experience** in the **Oncology (preferably solid tumors)** therapeutic area in the pharmaceutical industry
+ **Hands on experience** with **data review and clean, data analysis with extensive experience using EDC, CTMS and other database.**
+ Knowledge of **clinical trial methodology, regulatory and compliance requirements governing clinical trials and experience in the design of study protocols**
**Skills:**
+ **Oncology clinical trial experience** in the **Oncology (preferably solid tumors)** therapeutic area in the pharmaceutical industry
+ **Hands on experience** with **data review and clean, data analysis with extensive experience using EDC, CTMS and other database.**
+ Contribute to the **scientific content of Study Protocols, Investigator Brochures, Clinical Study Reports, Informed Consent Forms, briefing documents, charters, and regulatory documents.**
**Education:**
+ **Bachelors degree** in the sciences; advanced degree **(e.g., MS, PhD, PharmD)** preferred.
**About US Tech Solutions:**
US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Senior Clinical Scientist
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
As a Senior Clinical Scientist you will be joining the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence.
The Senior Clinical Scientist will work with the Study Medical Monitor/Study Clinical Scientist and provide scientific and clinical support from ongoing early and late-stage clinical trials with an emphasis on protocol-specific, in-life clinical data monitoring activities. This role will also serve as a point of contact for CROs, investigators and study staff in day-to-day safety monitoring under the guidance of the Study Medical Monitor. This individual will report into Global Clinical Operations and will interface directly with the Study Clinical Scientist and other cross-functional team members (including Clinical Development, Global Clinical Operations, Data Management, Biometrics, Patient Safety, Clinical Pharmacology and Biomarkers,) to support clinical study execution and clinical data monitoring.
**What you will be doing:**
+ Support Study Clinical Scientist in medical surveillance and medical monitoring activities under the guidance of the Medical Monitor; conduct daily medical surveillance of laboratory & ECG alerts including review of eligibility criteria as appropriate.
+ Provides analytical support of clinical trial data, including assessment and follow-up of issues relating to protocol conduct and/or individual subject safety.
+ Responsible for gathering, reviewing, and providing preliminary assessments of medical surveillance events to the Study Clinical Scientist and the Study Medical Monitor. Generate study safety events trackers, periodic medical monitoring reports and safety reviews in line with the needs of the study.
+ Participate in cross-functional study execution team activities relating to clinical data review.
+ Contribute to ICFs, training documents, and other clinical and regulatory documents under the direction of the Medical Monitor/Study Clinical Scientist as applicable.
+ Interact with internal and external stakeholders (study sites, vendors, etc.) in support of clinical trial objectives related to subject safety and clinical data monitoring; responds to or triages medical and safety-related questions for appropriate actions.
+ Performs other duties as assigned related to clinical programs.
**You are:**
+ Life sciences degree (BS, MS, or Ph.D.) with clinical or pre-clinical research experience in the pharmaceutical industry or healthcare setting.
+ Previous experience as a Clinical Scientist within a pharmaceutical, biotechnology, or CRO environment.
+ Experience in analysis and interpretation of clinical data (including safety and efficacy); working knowledge of GCP and clinical trial execution.
+ Experience working with clinical trial sites.
+ Experience in all stages of drug development.
+ Ability to make independent, timely and appropriate decisions.
+ Ability to handle multiple projects at a time and have a strong attention to detail Excellent oral and written communication skills and solid computer/analytical skills.
+ Ability to work collaboratively in a fast-paced, team-based matrix environment and to function independently as appropriate.
+ High level of organizational and project management skills.
+ Flexible to accommodate changes in team and project needs.
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply

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.
**Working at Abbott**
At Abbott, you can do work that matters, grow, and learn, care for yourself and your 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.
+ 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.
+ A company recognized as a great place to work in dozens of countries worldwide 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 the best place to work for diversity, working mothers, female executives, and scientists.
**The Opportunity**
This position works out of our SH division.
Structural Heart Business Mission: Why We Exist
Our business purpose is to restore health and improve quality of life by designing and providing device and management solutions for treating structural heart disease.
As the Principal Clinical Scientist, you'll have the chance to work closely with the clinical study team including project management, biostatistician, data management, and other clinical study personnel. This position will have significant interaction with leadership and regulatory authorities. Furthermore, this position will be required to execute their job responsibilities within the corporate policies and standard operating procedures.
**What You'll Work On**
+ Develops, writes, or mentors others in creation of clinical strategy, risk management, or clinical evaluation planning for products and process changes, to gain regulatory approval for product release, additional claims or indications, by addressing issues from a clinical, medical, and scientific perspective and by interacting with appropriate personnel.
+ Develops, writes, or mentors others in generation of study-related documents and/or contribute content and oversight of such documents, including, but not limited to, clinical study reports, clinical study protocols, case report forms, investigational brochures, and informed consent forms.
+ Designs or mentors others in the design of clinical trials and studies in collaboration with internal stake holders including clinical project management, clinical operations, biostatistics data management, regulatory affairs, medical affairs as well as external stake holders including steering and publication committees.
+ Develop the scientific podium and publication strategy in close collaboration with cross-functional teams and lead the execution of the publication strategy through coordination with investigator authors and internal teams.
+ Serve as an active member of study teams and provide scientific support to justify trial design and ongoing scientific analysis during protocol development. May include generation of pre-protocol documentation of scientific information.
+ Review and critically analyze statistical analysis plans.
+ Generate documents to support regulatory submissions for Abbott products and/or respond to questions from regulatory authorities about existing submissions.
**Required Qualifications**
+ Advanced degree in the sciences, medicine, or similar discipline.
+ 8+ years of related work experience with a solid understanding of specified functional area, or an equivalent combination of education and work experience.
+ Demonstrated scientific writing ability.
+ Will perform this job in a quality system environment. Failure to adequately perform tasks can result in noncompliance with governmental regulations.
+ Independent decision making required.
+ 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.
**Preferred Qualifications**
· PhD in a scientific, medical, or related discipline.
· Experience with regulated and post-market clinical studies.
· Familiarity with quality system environments.
· Strong background in medical device clinical trials.
· Knowledge of MDR requirements and experience developing PMCF Plans/Reports.
· Experience in physician and safety management.
· Prior collaboration with external clinical research committees (e.g., screening committees, DSMB, CEC).
Apply Now ( more about our health and wellness benefits, which provide the security to help you and your family live full lives:** ( 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.
The base pay for this position is $97,300.00 - $194,700.00. In specific locations, the pay range may vary from the range posted.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email

**Job Description Summary** **Job Description** **Role Summary/Purpose** As a Clinical Scientist, you will distinguish yourself through research collaboration within this Molecular Imaging technology. In close partnership with a PET and SPECT clinical and academic research partner - as well as GE HealthCare (GEHC) colleagues - you will be responsible for exploring, developing, and validating advanced imaging use and applications, ultimately expanding the translational impact of technology solutions in clinical practice to provide precision healthcare across the globe. **Essential Responsibilities** + Support large academic institution in the Great Lakes region in highly collaborative PET and SPECT clinical research with radiologists, physicists, technologists, and specialists. + Closely connect with GEHC global modality clinical and R&D teams, explore unmet clinical and technical needs with external collaborators identifying new research needs and building evidence. + Maintain and grow collaborator networks increasing connections between sites, driving insights into GEHC roadmap planning, and partnering with other functions (marketing, engineering, regulatory) for appropriate utilization of GE results. + Grow mindshare through joint scientific publications in peer-reviewed journals. + Provide support in pre- and post-market evidence generation, working with Research and Scientific Affairs to optimize collaborations and approach tied to GE product development needs and aligned institution interests. + Study new technology concepts and leverage expertise to move initiatives forward. + Assist in maturing evidence portfolio (writing journal publications/summary articles, technical documents, clinical marketing/training collaterals) and identifying unique opportunities for partnership (contributing to letters of support, research proposals, supporting identified grant submissions). + Drive adoption of new technology or clinical applications through advocacy and evidence. + Participate in presentations and scanner demonstrations regarding use of products for the institution's research purposes. + Support GEHC cross functional teams in providing educational services and training in response to academic site inquiries, serving as a technical product expert and prioritizing feedback. + Continuously grow clinical and technical expertise which may include participation in local or global congresses, mentoring, giving talks in small group or congress setting, connecting with other scientists, attending training, participating in internal development meetings, and staying abreast of new literature. **Qualifications/Requirements** + PhD plus 5 years' work experience in Physics, Chemistry, Life Sciences, Computer Science, Biomedical/Electrical/Software Engineering, or related field. + 3+ years of experience in medical imaging or closely related field, especially with expertise in PET or SPECT + Demonstrated record of innovation and development. + Excellent written and verbal communication skills. + Demonstrated clear thinking and problem-solving abilities and able to quickly grasp new ideas. + Self-starter, able to work independently and collaboratively, results oriented, able to multi-task. + Flexible, intellectually curious, and able to work with cross-functional, global teams. + Ability to work dynamically including from customer location, remote office, hospital or clinical site, and with ability to travel (<50%). + Adherence to practices related to Quality, Compliance, and Continuous Improvement + Focused experience in a specific clinical environment (e.g. radiology or cardiology department) including first authored peer reviewed articles + Familiarity with GE Imaging Systems and research on those systems. **Desired Characteristics** + Post Doc work in an engineering or science field such as Electrical Engineering, Biomedical Engineering, Computer Science, Applied Math or Physics, or equivalent focused in PET or SPECT + Proven customer relationship management and collaboration skills. + Experience in image reconstruction, analysis, and post-processing + Programming experience (e.g. in C/C++, Matlab) + Experience with academic and/or clinical research collaborations + Training in Good Clinical Practice (GCP), familiarity with and demonstrated practice of privacy, patient privacy, data controls GE HealthCare offers a great work environment, professional development, challenging careers, and competitive compensation. GE HealthCare is an Equal Opportunity Employer ( . Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law. GE HealthCare will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable). While GE HealthCare does not currently require U.S. employees to be vaccinated against COVID-19, some GE HealthCare customers have vaccination mandates that may apply to certain GE HealthCare employees. **Relocation Assistance Provided:** Yes