896 Research jobs

Are you a certified cytotechnologist? Are you in school pursuing a cytotechnologist degree/certification? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a full-time salaried cytotechnologist in a fast paced, customer focused, and challenging environment. LabCorp has a comprehensive benefits package and competitive compensation. LabCorp offers opportunities with advancement potential in an influential and expanding company. Be a part of something where you can make an impact on improving health and improving lives.   Specifically, you will perform the following:  Screens and evaluates any gynecologic and non-gynecologic specimens sent to the laboratory for the determination of possible malignant or related abnormal conditions  Ensures proper documentation of workload recording, including screening and non-screening activities as required by CLIA  Meets slide screening requirements as per standard operating procedure  Provides backup for cytology processing and other tasks as needed Requirements Requirements:  Cytotechnologist (CT) certified American Society for Clinical Pathology Board of Certification or equivalent  Bachelor of Science degree from an accredited college/university and documentation of one year of training at an accredited school of Cytotechnology  Able to work independently within a team and strong attention to detail  Proficient with computers  Demonstrated understanding of Cytopreparation techniques is recommended  Must pass CAP annual proficiency test  Automated and non-automated testing experience preferred  ThinPrep certification required  Surepath certified preferred  Must be able to pass a standardized color vision screen  Overtime required as business needs

Are you a certified cytotechnologist? Are you in school pursuing a cytotechnologist degree/certification? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a full-time salaried cytotechnologist in a fast paced, customer focused, and challenging environment. LabCorp has a comprehensive benefits package and competitive compensation. LabCorp offers opportunities with advancement potential in an influential and expanding company. Be a part of something where you can make an impact on improving health and improving lives.   Specifically, you will perform the following:  Screens and evaluates any gynecologic and non-gynecologic specimens sent to the laboratory for the determination of possible malignant or related abnormal conditions  Ensures proper documentation of workload recording, including screening and non-screening activities as required by CLIA  Meets slide screening requirements as per standard operating procedure  Provides backup for cytology processing and other tasks as needed Requirements Requirements:  Cytotechnologist (CT) certified American Society for Clinical Pathology Board of Certification or equivalent  Bachelor of Science degree from an accredited college/university and documentation of one year of training at an accredited school of Cytotechnology  Able to work independently within a team and strong attention to detail  Proficient with computers  Demonstrated understanding of Cytopreparation techniques is recommended  Must pass CAP annual proficiency test  Automated and non-automated testing experience preferred  ThinPrep certification required  Surepath certified preferred  Must be able to pass a standardized color vision screen  Overtime required as business needs

Are you a certified cytotechnologist? Are you in school pursuing a cytotechnologist degree/certification? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a full-time salaried cytotechnologist in a fast paced, customer focused, and challenging environment. LabCorp has a comprehensive benefits package and competitive compensation. LabCorp offers opportunities with advancement potential in an influential and expanding company. Be a part of something where you can make an impact on improving health and improving lives.   Specifically, you will perform the following:  Screens and evaluates any gynecologic and non-gynecologic specimens sent to the laboratory for the determination of possible malignant or related abnormal conditions  Ensures proper documentation of workload recording, including screening and non-screening activities as required by CLIA  Meets slide screening requirements as per standard operating procedure  Provides backup for cytology processing and other tasks as needed Requirements Requirements:  Cytotechnologist (CT) certified American Society for Clinical Pathology Board of Certification or equivalent  Bachelor of Science degree from an accredited college/university and documentation of one year of training at an accredited school of Cytotechnology  Able to work independently within a team and strong attention to detail  Proficient with computers  Demonstrated understanding of Cytopreparation techniques is recommended  Must pass CAP annual proficiency test  Automated and non-automated testing experience preferred  ThinPrep certification required  Surepath certified preferred  Must be able to pass a standardized color vision screen  Overtime required as business needs

Are you a certified cytotechnologist? Are you in school pursuing a cytotechnologist degree/certification? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a full-time salaried cytotechnologist in a fast paced, customer focused, and challenging environment. LabCorp has a comprehensive benefits package and competitive compensation. LabCorp offers opportunities with advancement potential in an influential and expanding company. Be a part of something where you can make an impact on improving health and improving lives.   Specifically, you will perform the following:  Screens and evaluates any gynecologic and non-gynecologic specimens sent to the laboratory for the determination of possible malignant or related abnormal conditions  Ensures proper documentation of workload recording, including screening and non-screening activities as required by CLIA  Meets slide screening requirements as per standard operating procedure  Provides backup for cytology processing and other tasks as needed Requirements Requirements:  Cytotechnologist (CT) certified American Society for Clinical Pathology Board of Certification or equivalent  Bachelor of Science degree from an accredited college/university and documentation of one year of training at an accredited school of Cytotechnology  Able to work independently within a team and strong attention to detail  Proficient with computers  Demonstrated understanding of Cytopreparation techniques is recommended  Must pass CAP annual proficiency test  Automated and non-automated testing experience preferred  ThinPrep certification required  Surepath certified preferred  Must be able to pass a standardized color vision screen  Overtime required as business needs

Are you a certified cytotechnologist? Are you in school pursuing a cytotechnologist degree/certification? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a full-time salaried cytotechnologist in a fast paced, customer focused, and challenging environment. LabCorp has a comprehensive benefits package and competitive compensation. LabCorp offers opportunities with advancement potential in an influential and expanding company. Be a part of something where you can make an impact on improving health and improving lives.   Specifically, you will perform the following:  Screens and evaluates any gynecologic and non-gynecologic specimens sent to the laboratory for the determination of possible malignant or related abnormal conditions  Ensures proper documentation of workload recording, including screening and non-screening activities as required by CLIA  Meets slide screening requirements as per standard operating procedure  Provides backup for cytology processing and other tasks as needed Requirements Requirements:  Cytotechnologist (CT) certified American Society for Clinical Pathology Board of Certification or equivalent  Bachelor of Science degree from an accredited college/university and documentation of one year of training at an accredited school of Cytotechnology  Able to work independently within a team and strong attention to detail  Proficient with computers  Demonstrated understanding of Cytopreparation techniques is recommended  Must pass CAP annual proficiency test  Automated and non-automated testing experience preferred  ThinPrep certification required  Surepath certified preferred  Must be able to pass a standardized color vision screen  Overtime required as business needs

Are you a certified cytotechnologist? Are you in school pursuing a cytotechnologist degree/certification? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a full-time salaried cytotechnologist in a fast paced, customer focused, and challenging environment. LabCorp has a comprehensive benefits package and competitive compensation. LabCorp offers opportunities with advancement potential in an influential and expanding company. Be a part of something where you can make an impact on improving health and improving lives.   Specifically, you will perform the following:  Screens and evaluates any gynecologic and non-gynecologic specimens sent to the laboratory for the determination of possible malignant or related abnormal conditions  Ensures proper documentation of workload recording, including screening and non-screening activities as required by CLIA  Meets slide screening requirements as per standard operating procedure  Provides backup for cytology processing and other tasks as needed Requirements Requirements:  Cytotechnologist (CT) certified American Society for Clinical Pathology Board of Certification or equivalent  Bachelor of Science degree from an accredited college/university and documentation of one year of training at an accredited school of Cytotechnology  Able to work independently within a team and strong attention to detail  Proficient with computers  Demonstrated understanding of Cytopreparation techniques is recommended  Must pass CAP annual proficiency test  Automated and non-automated testing experience preferred  ThinPrep certification required  Surepath certified preferred  Must be able to pass a standardized color vision screen  Overtime required as business needs

Are you a certified cytotechnologist? Are you in school pursuing a cytotechnologist degree/certification? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a full-time salaried cytotechnologist in a fast paced, customer focused, and challenging environment. LabCorp has a comprehensive benefits package and competitive compensation. LabCorp offers opportunities with advancement potential in an influential and expanding company. Be a part of something where you can make an impact on improving health and improving lives.   Specifically, you will perform the following:  Screens and evaluates any gynecologic and non-gynecologic specimens sent to the laboratory for the determination of possible malignant or related abnormal conditions  Ensures proper documentation of workload recording, including screening and non-screening activities as required by CLIA  Meets slide screening requirements as per standard operating procedure  Provides backup for cytology processing and other tasks as needed Requirements Requirements:  Cytotechnologist (CT) certified American Society for Clinical Pathology Board of Certification or equivalent  Bachelor of Science degree from an accredited college/university and documentation of one year of training at an accredited school of Cytotechnology  Able to work independently within a team and strong attention to detail  Proficient with computers  Demonstrated understanding of Cytopreparation techniques is recommended  Must pass CAP annual proficiency test  Automated and non-automated testing experience preferred  ThinPrep certification required  Surepath certified preferred  Must be able to pass a standardized color vision screen  Overtime required as business needs

Are you a certified cytotechnologist? Are you in school pursuing a cytotechnologist degree/certification? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a full-time salaried cytotechnologist in a fast paced, customer focused, and challenging environment. LabCorp has a comprehensive benefits package and competitive compensation. LabCorp offers opportunities with advancement potential in an influential and expanding company. Be a part of something where you can make an impact on improving health and improving lives.   Specifically, you will perform the following:  Screens and evaluates any gynecologic and non-gynecologic specimens sent to the laboratory for the determination of possible malignant or related abnormal conditions  Ensures proper documentation of workload recording, including screening and non-screening activities as required by CLIA  Meets slide screening requirements as per standard operating procedure  Provides backup for cytology processing and other tasks as needed Requirements Requirements:  Cytotechnologist (CT) certified American Society for Clinical Pathology Board of Certification or equivalent  Bachelor of Science degree from an accredited college/university and documentation of one year of training at an accredited school of Cytotechnology  Able to work independently within a team and strong attention to detail  Proficient with computers  Demonstrated understanding of Cytopreparation techniques is recommended  Must pass CAP annual proficiency test  Automated and non-automated testing experience preferred  ThinPrep certification required  Surepath certified preferred  Must be able to pass a standardized color vision screen  Overtime required as business needs

Are you a certified cytotechnologist? Are you in school pursuing a cytotechnologist degree/certification? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a full-time salaried cytotechnologist in a fast paced, customer focused, and challenging environment. LabCorp has a comprehensive benefits package and competitive compensation. LabCorp offers opportunities with advancement potential in an influential and expanding company. Be a part of something where you can make an impact on improving health and improving lives.   Specifically, you will perform the following:  Screens and evaluates any gynecologic and non-gynecologic specimens sent to the laboratory for the determination of possible malignant or related abnormal conditions  Ensures proper documentation of workload recording, including screening and non-screening activities as required by CLIA  Meets slide screening requirements as per standard operating procedure  Provides backup for cytology processing and other tasks as needed Requirements Requirements:  Cytotechnologist (CT) certified American Society for Clinical Pathology Board of Certification or equivalent  Bachelor of Science degree from an accredited college/university and documentation of one year of training at an accredited school of Cytotechnology  Able to work independently within a team and strong attention to detail  Proficient with computers  Demonstrated understanding of Cytopreparation techniques is recommended  Must pass CAP annual proficiency test  Automated and non-automated testing experience preferred  ThinPrep certification required  Surepath certified preferred  Must be able to pass a standardized color vision screen  Overtime required as business needs

Are you a certified cytotechnologist? Are you in school pursuing a cytotechnologist degree/certification? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a full-time salaried cytotechnologist in a fast paced, customer focused, and challenging environment. LabCorp has a comprehensive benefits package and competitive compensation. LabCorp offers opportunities with advancement potential in an influential and expanding company. Be a part of something where you can make an impact on improving health and improving lives.   Specifically, you will perform the following:  Screens and evaluates any gynecologic and non-gynecologic specimens sent to the laboratory for the determination of possible malignant or related abnormal conditions  Ensures proper documentation of workload recording, including screening and non-screening activities as required by CLIA  Meets slide screening requirements as per standard operating procedure  Provides backup for cytology processing and other tasks as needed Requirements Requirements:  Cytotechnologist (CT) certified American Society for Clinical Pathology Board of Certification or equivalent  Bachelor of Science degree from an accredited college/university and documentation of one year of training at an accredited school of Cytotechnology  Able to work independently within a team and strong attention to detail  Proficient with computers  Demonstrated understanding of Cytopreparation techniques is recommended  Must pass CAP annual proficiency test  Automated and non-automated testing experience preferred  ThinPrep certification required  Surepath certified preferred  Must be able to pass a standardized color vision screen  Overtime required as business needs

As you develop your career as a CRA, this role offers you the opportunity to plan and progress your career in the direction you choose. At IQVIA™ , we do not believe in a ‘career ceiling.’ You can make the Senior CRA role a stepping-stone into wider opportunities like operations management, dedicated customer solutions, and project management. And you won’t do it alone – you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards. Award winning and innovative, we will give you access to cutting-edge in-house technology, allowing you to work on global projects but with a regional / home state travel remit, so no need for national travel in certain countries. You will be building a smart and flexible career with no limits. While projects vary, your typical responsibilities might include: Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation Supporting the development of a subject recruitment plan Establishing regular lines of communication plus administering protocol and related study training to assigned sites Evaluating the quality and integrity of site practices – escalating quality issues as appropriate Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. Additional Description: You should have: A Bachelor's degree in a health care or other scientific discipline or educational equivalent At least two years of on-site monitoring experience Alternatively, you should have an equivalent combination of education, training and experience

As you develop your career as a CRA, this role offers you the opportunity to plan and progress your career in the direction you choose. At IQVIA™ , we do not believe in a ‘career ceiling.’ You can make the Senior CRA role a stepping-stone into wider opportunities like operations management, dedicated customer solutions, and project management. And you won’t do it alone – you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards. Award winning and innovative, we will give you access to cutting-edge in-house technology, allowing you to work on global projects but with a regional / home state travel remit, so no need for national travel in certain countries. You will be building a smart and flexible career with no limits. While projects vary, your typical responsibilities might include: Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation Supporting the development of a subject recruitment plan Establishing regular lines of communication plus administering protocol and related study training to assigned sites Evaluating the quality and integrity of site practices – escalating quality issues as appropriate Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. Additional Description: You should have: A Bachelor's degree in a health care or other scientific discipline or educational equivalent At least two years of on-site monitoring experience Alternatively, you should have an equivalent combination of education, training and experience

As you develop your career as a CRA, this role offers you the opportunity to plan and progress your career in the direction you choose. At IQVIA™ , we do not believe in a ‘career ceiling.’ You can make the Senior CRA role a stepping-stone into wider opportunities like operations management, dedicated customer solutions, and project management. And you won’t do it alone – you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards. Award winning and innovative, we will give you access to cutting-edge in-house technology, allowing you to work on global projects but with a regional / home state travel remit, so no need for national travel in certain countries. You will be building a smart and flexible career with no limits. While projects vary, your typical responsibilities might include: Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation Supporting the development of a subject recruitment plan Establishing regular lines of communication plus administering protocol and related study training to assigned sites Evaluating the quality and integrity of site practices – escalating quality issues as appropriate Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. Additional Description: You should have: A Bachelor's degree in a health care or other scientific discipline or educational equivalent At least two years of on-site monitoring experience Alternatively, you should have an equivalent combination of education, training and experience

As you develop your career as a CRA, this role offers you the opportunity to plan and progress your career in the direction you choose. At IQVIA™ , we do not believe in a ‘career ceiling.’ You can make the Senior CRA role a stepping-stone into wider opportunities like operations management, dedicated customer solutions, and project management. And you won’t do it alone – you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards. Award winning and innovative, we will give you access to cutting-edge in-house technology, allowing you to work on global projects but with a regional / home state travel remit, so no need for national travel in certain countries. You will be building a smart and flexible career with no limits. While projects vary, your typical responsibilities might include: Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation Supporting the development of a subject recruitment plan Establishing regular lines of communication plus administering protocol and related study training to assigned sites Evaluating the quality and integrity of site practices – escalating quality issues as appropriate Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. Additional Description: You should have: A Bachelor's degree in a health care or other scientific discipline or educational equivalent At least two years of on-site monitoring experience Alternatively, you should have an equivalent combination of education, training and experience

As you develop your career as a CRA, this role offers you the opportunity to plan and progress your career in the direction you choose. At IQVIA™ , we do not believe in a ‘career ceiling.’ You can make the Senior CRA role a stepping-stone into wider opportunities like operations management, dedicated customer solutions, and project management. And you won’t do it alone – you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards. Award winning and innovative, we will give you access to cutting-edge in-house technology, allowing you to work on global projects but with a regional / home state travel remit, so no need for national travel in certain countries. You will be building a smart and flexible career with no limits. While projects vary, your typical responsibilities might include: Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation Supporting the development of a subject recruitment plan Establishing regular lines of communication plus administering protocol and related study training to assigned sites Evaluating the quality and integrity of site practices – escalating quality issues as appropriate Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. Additional Description: You should have: A Bachelor's degree in a health care or other scientific discipline or educational equivalent At least two years of on-site monitoring experience Alternatively, you should have an equivalent combination of education, training and experience

As you develop your career as a CRA, this role offers you the opportunity to plan and progress your career in the direction you choose. At IQVIA™ , we do not believe in a ‘career ceiling.’ You can make the Senior CRA role a stepping-stone into wider opportunities like operations management, dedicated customer solutions, and project management. And you won’t do it alone – you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards. Award winning and innovative, we will give you access to cutting-edge in-house technology, allowing you to work on global projects but with a regional / home state travel remit, so no need for national travel in certain countries. You will be building a smart and flexible career with no limits. While projects vary, your typical responsibilities might include: Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation Supporting the development of a subject recruitment plan Establishing regular lines of communication plus administering protocol and related study training to assigned sites Evaluating the quality and integrity of site practices – escalating quality issues as appropriate Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. Additional Description: You should have: A Bachelor's degree in a health care or other scientific discipline or educational equivalent At least two years of on-site monitoring experience Alternatively, you should have an equivalent combination of education, training and experience

As you develop your career as a CRA, this role offers you the opportunity to plan and progress your career in the direction you choose. At IQVIA™ , we do not believe in a ‘career ceiling.’ You can make the Senior CRA role a stepping-stone into wider opportunities like operations management, dedicated customer solutions, and project management. And you won’t do it alone – you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards. Award winning and innovative, we will give you access to cutting-edge in-house technology, allowing you to work on global projects but with a regional / home state travel remit, so no need for national travel in certain countries. You will be building a smart and flexible career with no limits. While projects vary, your typical responsibilities might include: Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation Supporting the development of a subject recruitment plan Establishing regular lines of communication plus administering protocol and related study training to assigned sites Evaluating the quality and integrity of site practices – escalating quality issues as appropriate Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. Additional Description: You should have: A Bachelor's degree in a health care or other scientific discipline or educational equivalent At least two years of on-site monitoring experience Alternatively, you should have an equivalent combination of education, training and experience

As you develop your career as a CRA, this role offers you the opportunity to plan and progress your career in the direction you choose. At IQVIA™ , we do not believe in a ‘career ceiling.’ You can make the Senior CRA role a stepping-stone into wider opportunities like operations management, dedicated customer solutions, and project management. And you won’t do it alone – you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards. Award winning and innovative, we will give you access to cutting-edge in-house technology, allowing you to work on global projects but with a regional / home state travel remit, so no need for national travel in certain countries. You will be building a smart and flexible career with no limits. While projects vary, your typical responsibilities might include: Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation Supporting the development of a subject recruitment plan Establishing regular lines of communication plus administering protocol and related study training to assigned sites Evaluating the quality and integrity of site practices – escalating quality issues as appropriate Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. Additional Description: You should have: A Bachelor's degree in a health care or other scientific discipline or educational equivalent At least two years of on-site monitoring experience Alternatively, you should have an equivalent combination of education, training and experience

As you develop your career as a CRA, this role offers you the opportunity to plan and progress your career in the direction you choose. At IQVIA™ , we do not believe in a ‘career ceiling.’ You can make the Senior CRA role a stepping-stone into wider opportunities like operations management, dedicated customer solutions, and project management. And you won’t do it alone – you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards. Award winning and innovative, we will give you access to cutting-edge in-house technology, allowing you to work on global projects but with a regional / home state travel remit, so no need for national travel in certain countries. You will be building a smart and flexible career with no limits. While projects vary, your typical responsibilities might include: Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation Supporting the development of a subject recruitment plan Establishing regular lines of communication plus administering protocol and related study training to assigned sites Evaluating the quality and integrity of site practices – escalating quality issues as appropriate Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. Additional Description: You should have: A Bachelor's degree in a health care or other scientific discipline or educational equivalent At least two years of on-site monitoring experience Alternatively, you should have an equivalent combination of education, training and experience

At Myriad, we strive to be a trusted advisor to patients, their families and their healthcare professionals. “At Myriad, we are all about the patient. We work every day to provide the highest quality testing to our patients and always keep in mind that the results we provide are affecting the lives of our patients and their family members. I feel good knowing that we all share this common goal.” – Debbie, a Myriad Scientist for 10 years Our dedication to saving lives and improving the quality of life for patients drives our commitment to providing timely, accurate and actionable test results and ensuring that our genetic tests are available and affordable to those who need them. Myriad Women’s Health, is a leading personalized medicine company dedicated to being a trusted advisor transforming patient lives worldwide with pioneering molecular diagnostics. Myriad discovers and commercializes molecular diagnostic tests that: determine the risk of developing disease, accurately diagnose disease, assess the risk of disease progression, and guide treatment decisions across six major medical specialties where molecular diagnostics can significantly improve patient care and lower healthcare costs. Myriad is focused on three strategic imperatives: maintaining leadership in an expanding hereditary cancer market, diversifying its product portfolio through the introduction of new products and increasing the revenue contribution from international markets. For more information on how Myriad is making a difference, please visit the Company's website: www.myriad.com. Myriad is an equal opportunity employer and as such, affirms in policy and practice to recruit, hire, train and promote, in all job classifications without regard to race, color, religion, gender, age, sexual orientation, gender identity, national origin, disability status or status as a protected veteran. Reasonable accommodation will be provided for qualified individuals with disabilities and disabled veterans in job application procedures. We believe that diversity lends a regional, national, and global advantage to the clients we serve. Our workforce consists of dynamic individuals, with a range of backgrounds, talents, and skills.