Medical Director/Sr. Medical Director, Immunology Clinical Development – Gastroenterology

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          "text": "<p>Purpose:&#xa0;</p><p>​​With supervision, oversees the direction, planning, execution and interpretation of clinical trials or research activities of a clinical development program. Participates in cross-functional teams to generate, deliver, and interpret high-quality clinical data supporting overall product scientific and business&#xa0;strategy.​ &#xa0;</p><p>&#xa0;</p><p>Responsibilities:&#xa0;</p><p>​​•With appropriate supervision, manages 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. Oversees project-related education of investigators, study site personnel, and AbbVie study staff. &#xa0;<br>\n•Has 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, is responsible for oversight of study enrollment and overall timelines for key deliverables.  Responsible for assessment and reporting of serious adverse events per corporate policy and regulations for those protocols on which&#xa0;assigned. &#xa0;<br>\n•Contributes to design, analysis, interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses, and other program documents. &#xa0;<br>\n•May serve on a Clinical Strategy Team as the clinical representative for the protocols for which the incumbent has responsibility.  Contributes to the development of a rigorous, cross-functionally-aligned, vetted Clinical Development Plan in collaboration with matrix team members. &#xa0;<br>\n•Participates in opinion leader interactions related to the disease area(s); partners with Medical Affairs, Commercial and other functions in these activities as required, consistent with corporate policies. &#xa0;<br>\n•Stays abreast of professional information and technology through conferences, medical literature, and other available training, to augment expertise in the therapeutic area. &#xa0;<br>\n•Responsible for understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. May be asked to contribute to regulatory responses and discussions. &#xa0;<br>\n•Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality standards in conducting research. &#xa0;</p><p>&#xa0;</p>",
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          "text": "<p>Medical Director Qualifications: &#xa0;</p><p>•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&#xa0;strongly&#xa0;preferred.  Completion of a subspecialty fellowship&#xa0;in Gastroenterology&#xa0;is desirable. Experience&#xa0;in translational research is preferred.  &#xa0;</p><p>•Ability to run a clinical research study with&#xa0;appropriate supervision. &#xa0;</p><p>•Strong desire&#xa0;to collaborate in a cross-functional setting.&#xa0;</p><p>•Clinical trial experience in the pharmaceutical industry, academia, or equivalent is preferred. &#xa0;</p><p>•Knowledge of clinical trial&#xa0;methodology, regulatory and compliance requirements governing clinical trials and experience in the design of study protocols is desirable.&#xa0;</p><p>•Ability to interact externally and internally to support global scientific and business strategy. &#xa0;</p><p>•Must&#xa0;possess&#xa0;excellent oral and written English communication&#xa0;skills..&#xa0;</p><p>&#xa0;</p><p>Senior Medical Director Qualifications: &#xa0;</p><p>•Medical Doctor (M.D.), Doctor of Osteopathy (D.O.)&#xa0;or non-US equivalent of M.D. degree with relevant therapeutic specialty in an academic or hospital environment. Completion of a residency program&#xa0;strongly&#xa0;preferred.  Completion of a subspecialty fellowship&#xa0;in Gastroenterology&#xa0;is desirable.&#xa0;<br>\n•At least 2 years of clinical trial experience in the pharmaceutical industry, academia, or equivalent. Experience&#xa0;in translational research is preferred.  &#xa0;<br>\n•Ability to run a clinical research program of moderate complexity with minimal supervision.&#xa0;<br>\n•Ability to perform and bring out the best in others on a cross-functional global team.&#xa0;<br>\n•Ability to interact externally and internally to support a global scientific and business strategy.&#xa0;<br>\n•Knowledge of clinical trial&#xa0;methodology, regulatory and compliance requirements governing clinical trials and experience in development of clinical strategy and the design&#xa0;of study protocols.&#xa0;<br>\n•Must&#xa0;possess&#xa0;excellent oral and written English communication skills.&#xa0;</p>",
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          "text": "<p><strong>About AbbVie</strong></p><p>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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&#xa0;<a href=\"http://www.abbvie.com/\" rel=\"noopener noreferrer\">www.abbvie.com</a>. Follow @abbvie on&#xa0;<a href=\"https://www.linkedin.com/company/abbvie/\" rel=\"noopener noreferrer\">LinkedIn,</a>&#xa0;<a href=\"https://www.facebook.com/AbbVieGlobal/\" rel=\"noopener noreferrer\">Facebook</a>,&#xa0;<a href=\"https://www.instagram.com/abbvie/\" rel=\"noopener noreferrer\">Instagram</a>,&#xa0;<a href=\"https://twitter.com/abbvie\" rel=\"noopener noreferrer\">X</a>&#xa0;and&#xa0;<a href=\"https://www.youtube.com/user/AbbVie\" rel=\"noopener noreferrer\">YouTube.</a></p>",
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          "text": "<p>Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&#xa0;local law:&#xa0;​</p><ul><li>The compensation range described below is the range of possible base pay compensation that the Company&#xa0;believes in&#xa0;good faith it will pay for this role at the time&#xa0;of this posting based on the job grade for this position.&#xa0;Individual&#xa0;compensation paid within this range will depend on many factors including geographic location, and&#xa0;we&#xa0;may&#xa0;ultimately&#xa0;pay&#xa0;more or less than the posted range. This range may be&#xa0;modified&#xa0;in the&#xa0;future.&#xa0;​</li><li>We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&#xa0;medical/dental/vision&#xa0;insurance and 401(k) to eligible&#xa0;employees.​</li><li>This job is eligible to&#xa0;participate&#xa0;in our long-term incentive&#xa0;programs.&#xa0;</li></ul><p>Note: No amount of pay&#xa0;is considered to be&#xa0;wages or compensation until such amount is earned, vested, and&#xa0;determinable.&#xa0;The amount and availability of any bonus,&#xa0;commission, incentive, benefits, or any other form of&#xa0;compensation and benefits&#xa0;that are allocable to a particular employee&#xa0;remains&#xa0;in the Company's sole and&#xa0;absolute&#xa0;discretion unless and until paid and&#xa0;may be&#xa0;modified&#xa0;at the Company’s sole and absolute discretion, consistent with&#xa0;applicable law.​</p><div sr-tagline=\"\"></div><p>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.&#xa0;</p><p>US &amp; Puerto Rico only - to learn more, visit&#xa0;<a href=\"https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html\" rel=\"noopener noreferrer\">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html</a></p><p>US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:</p><p><a href=\"https://www.abbvie.com/join-us/reasonable-accommodations.html\" rel=\"noopener noreferrer\">https://www.abbvie.com/join-us/reasonable-accommodations.html</a></p>",
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