Haematology – Pipeline MSL

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    negotiable / month
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    7 hours ago
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**About AbbVie**

AbbVie (NYSE:ABBV) is a global, research-driven biopharmaceutical company committed to developing innovative advanced therapies for some of the world’s most complex and critical conditions. The company’s mission is to use its expertise, dedicated people and unique approach to innovation to markedly improve treatments across four primary therapeutic areas: immunology, oncology, virology and neuroscience. In more than 75 countries, AbbVie employees are working every day to advance health solutions for people around the world. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie at https://twitter.com/abbvie on Twitter, Facebook at https://www.facebook.com/AbbVieCareers/ or LinkedIn at https://www.linkedin.com/company/abbvie/jobs .​

**AbbVie** (NYSE:ABBV) is a global, research-based biopharmaceutical company formed in 2013 following separation from Abbott. The company’s mission is to use its expertise, dedicated people and unique approach to innovation to develop and market advanced therapies that address some of the world’s most complex and serious diseases. AbbVie employs approximately 25,000 people worldwide and markets medicines in more than 170 countries.

For more information, please visit www.abbvie.com at http://www.abbvie.com/ . Follow us on

**Summary of Job Description:**

This field-based Pipeline MSL position serves to enhance AbbVie’s scientific credibility with clinical investigators as well as key scientific institutions and collaborative study groups within the oncology/haematology therapy area (TA). The role will support scientific dialogue and collaborations in the areas of research, medical and scientific exchange and through the facilitation of requests for scientific and medical information. Aligned to AbbVie’s One R&D culture. it will also establish close partnerships with local Clinical Operations colleagues during the planning, initiation, oversight and follow-up of clinical study-related activities. The Pipeline MSL will also interface with other key members of the AbbVie ANZ medical department, including Medical Managers, Pharmacovigilence, Medical Information, Therapeutic Area Specialists and functions such as Market Access, Regulatory Affairs, Early Asset Teams and others as appropriate. The role will also work closely, collaboratively and cross-functionally with other in-field medical affairs members while retaining functional independence. The Pipeline MSL will also be required to maintain a high level of scientific knowledge to ensure credible dissemination of scientific information and informed scientific dialogue with key internal and external stakeholders.

**Major Responsibilities:**

+ Ensure a strong medical and scientific presence for AbbVie in investigational sites and key scientific centers by facilitation of clinical research and in particular of interventional phase 1-3 trials with AbbVie drugs, while supporting requests for medical and scientific information on products or areas of therapeutic interest to AbbVie

+ Establish and maintain a close working relationship with Site Management & Monitoring staff and partner in facilitating the initiation and conduct of prioritised AbbVie-led clinical trials.

+ Provide scientific and technical leadership to ensure professional and credible relationships with investigators.

+ Consult with physicians, pharmacists and other medical professionals to refer appropriate patients to Clinical Trial sites and review clinical practice topics as requested by the investigator or referring sites.

+ Act as the point of contact with thought leaders to facilitate investigator-initiated study (IIS) ideas with AbbVie pipeline assets and requests for support to the local and global medical teams as appropriate.

+ Deliver credible presentations on scientific matters in the disease area of responsibility and about AbbVie’s pipeline to investigators in AbbVie-sponsored interventional research.

+ Participate in the selection process to identify appropriately qualified external experts the Company would wish to engage in collaborative efforts – such as potential research collaborations, or educational and advisory roles (Advisory Boards, Congresses, Symposia, etc.); while ensuring a high level of scientific or educational integrity in these collaborative efforts.

+ Identify opportunities for R&D collaborations with key institutions and thought leaders and liaise with the Search& Evaluation team and Discovery or Clinical Development teams to facilitate further assessment.

+ Facilitate medical and scientific field intelligence – for example, maintain a list of investigators/potential investigators within a given TA, understand competitive research activities in active or planned study sites, generate insights from investigators on challenges and opportunities for AbbVie-sponsored clinical trials– and communicate, where appropriate, within the Company.

+ Attend relevant scientific meetings and Conferences.

+ Upon request, assist physicians with requests for access to AbbVie medicines on a named patient or compassionate use basis, subject to all applicable legal and regulatory requirements.

+ Ensure that all activities and interactions are conducted with due regard to all applicable local, global and national laws, regulations, guidelines, codes of conduct, Company policies and accepted standards of best practice.

+ To provide insights on the current clinical practice, facilitate identification of top tier external experts and provide scientific input into the future clinical development program for AbbVie’s pipeline assets


**Education/Experience Required:**

+ Advanced degree (e.g. PharmD, MD, MBBS, PhD) in a relevant scientific discipline is strongly preferred but candidates with an undergraduate degree in a relevant discipline and demonstrated experience will be considered.

+ Experience in developing and maintaining expert knowledge for the assigned therapeutic area, and in medical research in general.

+ Professional experience as MSL or CRA or in a similar field-based R&D role for at least two years.

+ Solid knowledge of the pharmaceutical environment and the role of Medical Affairs to advance the medical and scientific objectives of a pharmaceutical company.

+ Experience as an active contributor to cross-functional teams and/or working in matrix organisations.

**Essential Skills & Abilities:**

+ Keen interest in developing and maintaining expert knowledge for assigned therapeutic area/product and in medical research in general

+ Excellentwritten and spoken communication and presentation skills.

+ Fluencyin written and oral English in order to facilitate communications betweenthe affiliate medical department, Regional and International MedicalAffairs and other AbbVie functional staff.

+ Highcustomer orientation.

+ Strongcommitment to compliance with the relevant rules and procedures, and toscientific quality and integrity.

+ Collaborative,team-oriented approach, able to develop and support relationships acrossan organisation as well as with key external stakeholders and thehealthcare community at large.

+ Demonstratedexpertise in the scientific methods applied to clinical research andcurrent legislative/regulatory controls applicable to this research.

+ Abilityto comprehensively learn about new subject areas and environments.

+ Soundjudgment, strong planning and organisational skills, and the ability toget things done.

+ Abilityto work independently, with limited guidance/oversight.


Yes, 75 % of the Time

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**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.