What are the responsibilities and job description for the Medical Science LiaisonSenior Medical Science Liaison - Immunology and Gene Therapy - Northeast position at EVERSANA?

This Medical Science Liaison / Senior Medical Science Liaison functions as a highly trained fieldbased scientific expert in gene therapy who engages health care professionals and leaders in clinical scientific valuebased care and researchbased peer to peer scientific exchange around recurrent respiratory papillomatosis (RRP). Following regulatory and corporate guidelines they will facilitate and build scientific relationships and collaborations with the Otolaryngology and Gene Therapy scientific communities. This position interacts with local regional and national Key Opinion Leaders (KOLs) and health care practitioners (HCPs) as well as professional societies and organizations. The MSL will need to be fully engaged with pertinent professional societies as well as other valuebased institutions and associations including clinics and centers that are involved with the treatment of recurrent respiratory papillomatosis (RRP) and centers that deliver gene therapy. The MSL will be the field based scientific expert regarding an offtheshelf (OTS) AdenoVerse gene therapy in patients with recurrent respiratory papillomatosis (RRP).

ESSENTIAL DUTIES AND RESPONSIBILITIES :

Function as the primary medical point of contact in geographic area. .
Maintain clinical and scientific expertise in otolaryngology pathophysiology and gene therapy with specific focus in standards of care related to the treatment of RRP.
Engage in well informed compliant robust and accurate scientific peer exchange around the company pipeline with KOLs .
Have a thorough understanding of the clinical protocols clinical trials outcomes and related procedures.
Develop and track key opinion leader (KOL) engagement plans identify develop and maintain longterm collaborative relationships with KOLs within assigned region.
Engage in medical & scientific exchange with the medical / scientific community including advisory boards.
Responsible for ongoing territory management and development
Responsible for all clinical program requests and for unsolicited requests for information.

May collaborate with R&D Team to support sites and investigators participating in the companysponsored clinical trials.

Conduct prelaunch KOL profiling efforts to enhance depth of product / disease / scientific knowledge. Facilitate top account / institution profiling efforts to enhance understanding of patient care pathways including treatment protocol development and novel therapies.

Work collaboratively and compliantly with commercial colleagues to assure product strategic imperatives are represented cross functionally in account engagement

Respond to and document unsolicited requests for information on clinical initiatives.

May serve as a resource for investigator sponsored trial (IST) proposal

Provide internal teams with feedback and insights from interactions with KOLs.

Represent company at medical meetings through Medical Affairs Scientific Booth coverage and other related activities.

Attend congresses as appropriate and develop meaningful internal reports of the congresses covered.

Adhere to corporate SOPs and ensure vigilant compliance with relevant legal and regulatory guidelines governing scientific interactions with physicians and healthcare professionals across all activities including those related to clinical trials scientific interactions with internal and external groups and responses to unsolicited requests for medical / scientific information.

Consistently demonstrate a high standard of excellence in the management of assigned territory while also contributing to the success of colleagues and the MSL team.

Willingness to contribute to the achievement of organizational goals beyond the borders of a geographic territory.

Be solidly versed in the clinical data such that the full range of innovative science clinical outcome economic and value aspects of company s products can be appreciated by the healthcare practitioner formulary member or payer.

Provide medical support clinical input and / or training for internal teams as requested.

Qualifications :

PREFERRED QUALIFICATIONS :

An advanced degree (e.g. PharmD PhD MD MSN or NP / PA) is required.

MSL : A minimum of 2 years previous MSL experience necessary with a minimum of 1 year in rare disease oncology (and / or immunology) with working knowledge of Gene Therapy.

Sr. MSL : A minimum of 5 years of pharma experience and 3 years of rare disease oncology (and / or immunology) experience.

Cell and Gene Therapy experience strongly preferred.

Prior product launch experience required.

Exhibits the highest level of scientific business and clinical acumen with excellent communication and networking skills.

The ability to interpret and present scientific data to engage KOLs.

Working knowledge of standards of care for RRP is desirable.

Previous experience sharing scientific content with payer systems is highly desirable.

Working knowledge of NCI Cooperative Groups and Oncology Research Consortiums

Ability to present complex scientific and value and evidence data to payors and / or formulary committees is required.

Working knowledge of institutions and clinics in selected geographies is expected.

Excellent written and oral presentation skills.

Ability to travel frequently (70%) with overnight stays (e.g. KOL meetings site locations internal meetings medical meetings and congresses training).

Additional Information :

OUR CULTURAL BELIEFS

Patient Minded I act with the patients best interest in mind.

Client Delight I own every client experience and its impact on results.

Take Action I am empowered and hold myself accountable.

Embrace Diversity I create an environment of awareness and respect.

Grow Talent I own my development and invest in the development of others.

Win Together I passionately connect with anyone anywhere anytime to achieve results.

Communication Matters I speak up to create transparent thoughtful and timely dialogue.

Always Innovate I am bold and creative in everything I do.

Our team is aware of recent fraudulent job offers in the market misrepresenting EVERSANA. Recruitment fraud is a sophisticated scam commonly perpetrated through online services using fake websites unsolicited emails or even text messages claiming to be a legitimate company. Some of these scams request personal information and even payment for training or job application fees. Please know EVERSANA would never require personal information nor payment of any kind during the employment process. We respect the personal rights of all candidates looking to explore careers at EVERSANA.

From EVERSANAs inception Diversity Equity & Inclusion have always been key to our success. We are an Equal Opportunity Employer and our employees are people with different strengths experiences and backgrounds who share a passion for improving the lives of patients and leading innovation within the healthcare industry. Diversity not only includes race and gender identity but also age disability status veteran status sexual orientation religion and many other parts of ones identity. All of our employees points of view are key to our success and inclusion is everyones responsibility.

Consistent with the Americans with Disabilities Act (ADA) and applicable state and local laws it is the policy of EVERSANA to provide reasonable accommodation when requested by a qualified applicant or candidate with a disability unless such accommodation would cause an undue hardship for EVERSANA. The policy regarding requests for reasonable accommodations applies to all aspects of the hiring process. If reasonable accommodation is needed to participate in the interview and hiring process please contact us at .

Remote Work : Employment Type :

Fulltime

Key Skills

Presentation Skills,Time Management,Clinical Research,Communication skills,GCP,Infusion Experience,Managed Care,Hospice Care,Conflict Management,Clinical Trials,Research Experience,Home Care

Experience : years

Vacancy : 1

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