AbbVie
Medical Director Obesity and Endocrinology Clinical Development
AbbVie, North Chicago, Illinois, us, 60086
Medical Director Obesity and Endocrinology Clinical Development
AbbVie - Position at AbbVie Base pay range
$156,000.00/yr - $296,500.00/yr Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit www.abbvie.com. Purpose
With supervision, oversee the direction, planning, execution, and interpretation of clinical trials or research activities of one or more clinical development programs. Participate in and may lead cross‑functional teams to generate, deliver, and disseminate high‑quality clinical data supporting the overall product scientific and business strategy. Responsibilities
With appropriate supervision, manage the design and implementation of study protocols for a clinical development program in support of the overall Product Development Plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie’s customers, markets, business operations and emerging issues. Oversee project‑related education of investigators, study site personnel and AbbVie study staff. Have responsibility for oversight of clinical studies, monitoring overall study integrity and review, interpretation and communication of accumulating data pertaining to safety and efficacy of the molecule. Along with Clinical Operations, oversee study enrollment and overall timelines for key deliverables. Contribute to design, analysis, interpretation and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses and other program documents. May serve on a Clinical Strategy Team as the clinical representative for the protocols for which the incumbent has responsibility. Participate in opinion leader interactions related to the disease area(s); partner with Medical Affairs, Commercial and other functions as required, consistent with corporate policies. Stay abreast of professional information and technology through conferences, medical literature and other available training, to augment expertise in the therapeutic area. Responsible for understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. Ensure adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality standards in conducting research. Qualifications
Medical Doctor (M.D.), Doctor of Osteopathy (D.O.) or non‑US equivalent of M.D. degree with relevant therapeutic specialty in an academic or hospital environment. Completion of a residency program strongly preferred. Completion of a subspecialty fellowship is desirable. Ability to run a clinical research study with appropriate supervision. Strong desire to collaborate in a cross‑functional setting. Clinical trial experience in the pharmaceutical industry, academia, or equivalent is preferred. Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials and experience in the design of study protocols is desirable. Ability to interact externally and internally to support global scientific and business strategy. Must possess excellent oral and written English communication skills. Additional Information
The compensation range described above represents the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of the posting. We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. This job is eligible to participate in our short‑term incentive programs. This job is eligible to participate in our long‑term incentive programs. Equal Opportunity
AbbVie is an equal‑opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only – to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html. Accommodation
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html
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AbbVie - Position at AbbVie Base pay range
$156,000.00/yr - $296,500.00/yr Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit www.abbvie.com. Purpose
With supervision, oversee the direction, planning, execution, and interpretation of clinical trials or research activities of one or more clinical development programs. Participate in and may lead cross‑functional teams to generate, deliver, and disseminate high‑quality clinical data supporting the overall product scientific and business strategy. Responsibilities
With appropriate supervision, manage the design and implementation of study protocols for a clinical development program in support of the overall Product Development Plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie’s customers, markets, business operations and emerging issues. Oversee project‑related education of investigators, study site personnel and AbbVie study staff. Have responsibility for oversight of clinical studies, monitoring overall study integrity and review, interpretation and communication of accumulating data pertaining to safety and efficacy of the molecule. Along with Clinical Operations, oversee study enrollment and overall timelines for key deliverables. Contribute to design, analysis, interpretation and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses and other program documents. May serve on a Clinical Strategy Team as the clinical representative for the protocols for which the incumbent has responsibility. Participate in opinion leader interactions related to the disease area(s); partner with Medical Affairs, Commercial and other functions as required, consistent with corporate policies. Stay abreast of professional information and technology through conferences, medical literature and other available training, to augment expertise in the therapeutic area. Responsible for understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. Ensure adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality standards in conducting research. Qualifications
Medical Doctor (M.D.), Doctor of Osteopathy (D.O.) or non‑US equivalent of M.D. degree with relevant therapeutic specialty in an academic or hospital environment. Completion of a residency program strongly preferred. Completion of a subspecialty fellowship is desirable. Ability to run a clinical research study with appropriate supervision. Strong desire to collaborate in a cross‑functional setting. Clinical trial experience in the pharmaceutical industry, academia, or equivalent is preferred. Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials and experience in the design of study protocols is desirable. Ability to interact externally and internally to support global scientific and business strategy. Must possess excellent oral and written English communication skills. Additional Information
The compensation range described above represents the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of the posting. We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. This job is eligible to participate in our short‑term incentive programs. This job is eligible to participate in our long‑term incentive programs. Equal Opportunity
AbbVie is an equal‑opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only – to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html. Accommodation
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html
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