AbbVie

External Clinical Lead, Medical Affairs (Plastic Surgery and Regenerative Medicine)

Posted on: 11 Feb 2021

Madison, NJ

Job Description

About AbbVie
AbbVies mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on peoples lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, womens health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn.

Envision working with energetic colleagues and inspirational leaders. Now, place yourself in that mix; leading discussions, asking the right questions and driving results.

What Your New Manager Wants You To Know

The External Clinical Lead develops and maintains professional relationships with internal and external customers to provide comprehensive medical and scientific support for AbbVie initiatives in assigned therapeutic areas.

Facilitates information, education, and research activities for physicians and ancillary healthcare professionals regarding current and future therapies in development or commercialized by AbbVie. Provide scientific expertise and serve as a point of contact for both external experts and internal leads in Plastics and Regenerative Medicine (PRM). Ensures an aligned global medical and scientific strategy for products in PRM, working closely with GMA colleagues in Patient safety, global evidence & value (GE&V;), External Scientific Communications in addition to research and development colleagues and commercial colleagues. Provide scientific insights and expertise to help inform global strategic planning for PRM.

Additional activities, special projects and assignments may be given, as required. As a result, the percentage of time spent across key duties and responsibilities will vary depending on project assignments, therapeutic area needs and the requirements within GMA SP.

YOU ARE more than just a title, YOU ARE

* A strategic thinker: align and excite internal stakeholders to facilitate success through strong leadership, strategic thinking and personal drive.
* First class team player: collaborate across multiple disciplines to ensure compliance and ability to influence cross-functional teams and senior leadership.

You Will

External Relationships

* Identify, establish and maintain relationships with top tier thought leaders in the respective therapeutic area to establish a strong scientific presence in the clinical and academic communities. Ensure thought leader development and communication is optimized. Collaborate cross-functionally to establish scientific and clinical credibility with payers, managed market/market access and healthcare decision makers.
* Provide meaningful and comprehensive, external scientific communications both proactively and reactively.
* Deliver assigned portfolio-related clinical presentations and participate in prioritized scientific meetings and congresses.
* Execute GMA SP Advisory Boards (face-to-face and virtual) based on scientific need and TA strategic plan.
* Support advocacy development efforts.
* Support global strategic plan country level scientific information needs.
* Synthesize external insights to inform AbbVie PRM strategy (e.g. strategic insights, customer interactions).

Medical and Scientific Data Generation and Internal Communication

* Contribute to the development and review of trial proposals and publications.
* Contribute to the creation of materials and content used in scientific communications.
* Scientific training of new cross-functional hires as needed.
* Establish and maintain internal organizational links with the broader R&D;, Commercial and other AbbVie departments.
* Contribute to Commercial planning by leveraging medical/scientific expertise, knowledge of scientific data and understanding of the external healthcare environment.

Strategic and Tactical Planning

* Contribute to the development and responsible for the implementation of the TA Medical Affairs strategic and tactical plans.
* Deliver and communicate progress on project milestones.
* Contribute to the planning and execution of broader GMA functional activities that support the TA Medical Affairs strategic plans.
* Support assigned Core teams involving products within the TA as needed.
* Contribute to assigned sub-teams.
* Represent GMA on Clinical teams as needed

LI-PD1

Qualifications
You Bring

* MD degree from an accredited US or foreign medical school with postgraduate medical training required. PhD with relevant industry experience will be considered.
* Subspecialty training in the Therapeutic Area and/or industry experience in the field is preferred.
* Must have an understanding of legal and regulatory guidelines (e.g. knowledge of OPDP promotional regulations, CDER/CBER regulations as they relate to drug approvals).
* Understanding of Good Clinical Practices, ICH guidelines, PhRMA code, FDA CFR, ISO, clinical research ethics, HIPAA and patient privacy laws, EU Directive and other applicable local regulations
* Familiar with Medical Affairs principles, study design and publications.
* Proficient with electronic systems including Microsoft Office Suite, SharePoint, videoconferencing platforms

In this role, were looking for a leader who will:

* Act as an Owner
* Be Excellence Focused
* Act as an Influencer

Significant Work Activities
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)
Travel
No
Job Type
Experienced
Schedule
Full-time
Job Level Code
IC
Equal Employment Opportunity
At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic.

AbbVie

Chicago, IL

AbbVie Inc. discovers, develops, manufactures, and sells pharmaceutical products in the United States, Japan, Germany, Canada, Italy, Spain, the Netherlands, the United Kingdom, Brazil, and internationally. The company offers HUMIRA, a therapy administered as an injection for autoimmune and intestinal Behçet's diseases; IMBRUVICA to treat adult patients with chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL), mantle cell lymphoma, waldenström’s macroglobulinemia, marginal zone lymphoma, and chronic graft versus host disease; VENCLEXTA, a BCL-2 inhibitor used to treat adults with CLL or SLL; VIEKIRA PAK, an interferon-free therapy to treat adults with genotype 1 chronic hepatitis C virus (HCV); TECHNIVIE to treat adults with genotype 4 HCV infection; and MAVYRET to treat patients with chronic HCV genotype 1-6 infection.

It also provides KALETRA, an anti-human immunodeficiency virus (HIV)-1 medicine used with other anti-HIV-1 medications to maintain viral suppression in HIV-1 patients; NORVIR, a protease inhibitor indicated in combination with other antiretroviral agents to treat HIV-1; and SYNAGIS to prevent respiratory syncytial virus infection at-risk infants. In addition, the company offers AndroGel, a testosterone replacement therapy for males; CREON, a pancreatic enzyme therapy for exocrine pancreatic insufficiency; Synthroid to treat hypothyroidism; and Lupron to treat prostate cancer, endometriosis, and central precocious puberty, as well as anemia.

Further, it provides Duopa and Duodopa, a levodopa-carbidopa intestinal gel to treat Parkinson’s disease; Sevoflurane, an anesthesia product; and ORILISSA, a non-peptide small molecule gonadotropin-releasing hormone antagonist for women with moderate to severe endometriosis pain. It has collaborations with Alector, Inc.; Janssen Biotech, Inc.; Galapagos; Bristol-Myers Squibb Company; and Calico Life Sciences LLC. The company was incorporated in 2012 and is headquartered in North Chicago, Illinois.