Abbott Laboratories
Associate Clinical Site Lead – Northern CA
Abbott Laboratories, Alameda, California, United States, 94501
About AbbottAbbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.Working at AbbottAt 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.Health care and well-being programs including medical, dental, vision, wellness, and occupational health programs.Tuition reimbursement, the
Freedom 2 Save
student debt program and
FreeU
education benefit.A company recognized as a great place to work in dozens of countries around the world.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.The OpportunityThe
Associate Clinical Site Lead
for the Northern California region drives study execution and operational excellence across Abbott Cardiovascular therapies. Developing skills and foundation to become a resource in protocol execution, developing product and disease state knowledge, procedure support, clinical trial enrollment, and ICH-GCP and clinical research application.Adheres to specified site nomination, qualification, and startup processes. Leads ongoing training/retraining of all site stakeholders to ensure protocol adherence. Continuously reviews, manages, and influences all aspects of site’s recruitment and data collection performance. Proactively utilizes appropriate operational metrics to minimize screen failure and attrition rate. Monitors to ensure compliance with applicable regulatory requirements, Good Clinical Practice, and accuracy standards.What You'll Work OnWith supervision of senior colleague/manager:Develop and maintain a productive clinical territory:Identify, develop, and maintain sites capable of delivering start-up goals.Understand and assess investigators’ interests and qualifications.Maintain open communication and relationships with key site personnel.Provide ongoing technical support to customers and field staff.Facilitate communication between clinical sites and other Abbott clinical staff.Manage all aspects of study lifecycle to include site regulatory and quality:Start Up
Nominate, approach, and complete qualification processes.Facilitate all aspects of the start-up process.Train facility staff regarding protocol requirements.
Enrollment
Develop site-specific strategies to promote appropriate patient enrollment.Continuously evaluate site study performance and provide timely feedback.
Regulatory and Quality
Strong understanding of GCP and commitment to progress knowledge.Educate site on tools to facilitate compliance.Review data and source documentation from investigational sites.
Provide training and procedure coverage:Apply clinical and technical expertise to train site and Abbott staff.Attend study procedures and follow-ups.Collaborate with commercial partners:Collaborate in the education of local sales groups.Meet with key customers to enhance the customer experience.Identify and adapt to shifting priorities and competing demands.Maintain at least one area of expertise.Develop working knowledge of disease states and product lines.Education and Experience You’ll Bring:RequiredAssociate’s degreeMinimum 1 year experiencePreferredBachelor’s Degree in a related field, OR equivalent experience in cardiology or clinical research.2 years of progressively more responsible relevant clinical trial experience.Competency in catheterization lab and operating room protocol.Apply NowLearn more about our health and wellness benefits:
www.abbottbenefits.comFollow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future. Abbott is an Equal Opportunity Employer, committed to employee diversity.Connect with us at
www.abbott.com
and on social media.The base pay for this position is $48,000.00 – $96,000.00. In specific locations, the pay range may vary.
#J-18808-Ljbffr
Freedom 2 Save
student debt program and
FreeU
education benefit.A company recognized as a great place to work in dozens of countries around the world.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.The OpportunityThe
Associate Clinical Site Lead
for the Northern California region drives study execution and operational excellence across Abbott Cardiovascular therapies. Developing skills and foundation to become a resource in protocol execution, developing product and disease state knowledge, procedure support, clinical trial enrollment, and ICH-GCP and clinical research application.Adheres to specified site nomination, qualification, and startup processes. Leads ongoing training/retraining of all site stakeholders to ensure protocol adherence. Continuously reviews, manages, and influences all aspects of site’s recruitment and data collection performance. Proactively utilizes appropriate operational metrics to minimize screen failure and attrition rate. Monitors to ensure compliance with applicable regulatory requirements, Good Clinical Practice, and accuracy standards.What You'll Work OnWith supervision of senior colleague/manager:Develop and maintain a productive clinical territory:Identify, develop, and maintain sites capable of delivering start-up goals.Understand and assess investigators’ interests and qualifications.Maintain open communication and relationships with key site personnel.Provide ongoing technical support to customers and field staff.Facilitate communication between clinical sites and other Abbott clinical staff.Manage all aspects of study lifecycle to include site regulatory and quality:Start Up
Nominate, approach, and complete qualification processes.Facilitate all aspects of the start-up process.Train facility staff regarding protocol requirements.
Enrollment
Develop site-specific strategies to promote appropriate patient enrollment.Continuously evaluate site study performance and provide timely feedback.
Regulatory and Quality
Strong understanding of GCP and commitment to progress knowledge.Educate site on tools to facilitate compliance.Review data and source documentation from investigational sites.
Provide training and procedure coverage:Apply clinical and technical expertise to train site and Abbott staff.Attend study procedures and follow-ups.Collaborate with commercial partners:Collaborate in the education of local sales groups.Meet with key customers to enhance the customer experience.Identify and adapt to shifting priorities and competing demands.Maintain at least one area of expertise.Develop working knowledge of disease states and product lines.Education and Experience You’ll Bring:RequiredAssociate’s degreeMinimum 1 year experiencePreferredBachelor’s Degree in a related field, OR equivalent experience in cardiology or clinical research.2 years of progressively more responsible relevant clinical trial experience.Competency in catheterization lab and operating room protocol.Apply NowLearn more about our health and wellness benefits:
www.abbottbenefits.comFollow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future. Abbott is an Equal Opportunity Employer, committed to employee diversity.Connect with us at
www.abbott.com
and on social media.The base pay for this position is $48,000.00 – $96,000.00. In specific locations, the pay range may vary.
#J-18808-Ljbffr