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Home Flexible Job Board Molecular Oncology Specialist (Sales)

$130,000–165,000/yr 12d ago

Molecular Oncology Specialist (Sales)

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Agendia Inc.

Baltimore, MD, US

Full-time Permanent Remote

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Summary

The Molecular Oncology Specialist is responsible for developing and executing sales strategies to achieve revenue goals for oncology products within an assigned territory. They will identify, educate, and manage relationships with key stakeholders including oncologists, surgeons, and hospitals.

Job Description

Description

**Starting at $250k inclusive of Base Salary + Comm 

AIM OF THE POSITION

The Molecular Oncology Specialist’s (MOS) primary responsibilities are to develop and successfully execute sales strategies to ensure achievement of revenue goals for oncology services by focusing on strategic selling opportunities of Agendia franchise products (i.e. MammaPrint, BluePrint, etc.) within an assigned territory:  DC/Virginia/Maryland and a small portion of Southern Delaware  

POSITION WITHIN THE ORGANIZATION

1. Reports to Regional Sales Director

2. Cooperates with all departments

3. Participates in:

– Meetings

– Conferences

Trainings 

Requirements

ESSENTIAL DUTIES AND RESPONSIBILITIES

· Identify, target, educate and manage accounts in the assigned territory including hospitals, pathology groups, oncologists, and surgeons on Agendia’s products.

· Analyze the designated territory to understand prescribing and purchasing decision processes and any marked differences from national trends

· Drive new oncology business, maintaining customer relationships and exceeding sales targets

· Achieve sales forecasts and targets

· Participate in organizing and facilitating meetings for the exchange of medical and product information in line with the company’s policies, regulatory and legal requirements

· Represent company at trade shows, attend company meetings, training programs and functions as needed

· Recognize changes in the work environment, develop and implement alternate plans to achieve objectives, modify call plan/business plan activities accordingly

· Identify key physicians, health care providers and organizations within assigned territory

· Focus targeted sales activity on high-end revenue, volume opportunities, and on Community Based Oncology and Surgery practices

· Support company sales strategy and contribute in fostering a team environment

· Present a positive and professional image of Agendia, and ensure activities are consistent with and enhance the company’s ethical marketing policies and procedures.

· Travel independently throughout defined territory to drive oncology sales

· Develop and maintain relationships with Key Opinion Leaders (KOLs)

· Provide ongoing communication to the Regional Sales Director regarding business opportunities and issues.

· Maintain database of customers and targets in SFDC. (sales force)

· Present at quarterly sales meetings

· Work closely with marketing on regional market trends, competitive threats and new testing opportunities

· Follows all Agendia, Inc.’s health and safety policies and procedures

· Performs all Company business in accordance with all regulations (e.g., EEO, FDA, DEA, OSHA, PDMA, EPA, etc.) and Company policy and procedures. When violations are noted/observed they are to be immediately reported to management. Demonstrates high ethical and professional standards with all business contacts in order to maintain Agendia’s reputation within the medical community.

· Reside in the territory/geography is which they are assigned to.

· Provides consistent, timely and complete administrative duties and responsibilities. All expense reports, call reports, and communications are completed effectively and on time.

· Performs other related duties as required or assigned

· An MOS can provide test report orientation guidance at the request of the clinician, however should avoid making specific patient management or treatment recommendations.

The above listing represents the general duties considered essential functions of the job and is not to be considered a detailed description of all the work requirements that may be inherent in the position.

KEY CONTACTS

Internal: All departments

External: Physicians, Hospitals, Medical Centers, etc.

EDUCATION AND EXPERIENCE REQUIREMENTS

EDUCATION

· Bachelor’s degree, Master’s degree highly desired

EXPERIENCE

· 3 + years work experience in field sales, in the diagnostic, oncology, lab services, pharmaceutical, biotech, or other related industry

· Advanced knowledge of concepts and practices with the ability to use in diverse business situations

· Completing and implementing attainable business plans

KNOWLEDGE, SKILLS AND ABILITIES (KSA’S)

Specific Knowledge Required:

Knowledge: Comprehension of a body of information acquired by experience or study.

Skill: A present, observable competence to perform a learned activity.

Ability: Competence to perform an observable behavior.

· Demonstrate abilities to establish physicians thought leader and other relevant stakeholder relationships.

· Proven track record for consistently meeting or exceeding financial and/or other quantitative targets, as well as qualitative goals.

· Ability to communicate effectively and professionally with all members of the organization, customers and external contacts.

· Ability to travel with overnights and attendance at some weekend programs.

· Ability to translate key scientific information supporting product, competitors, science and marketplace to a broad range of Oncology customers.

· Ability to Reside in the territory/geography is which they are assigned to.

The above listing represents the general duties considered essential functions of the job and is not to be considered a detailed description of all the work requirements that may be inherent in the position.

BEHAVIOURAL COMPETENCIES/DESIRED SKILLS

· Self-Starter

· Ability to work independently and prioritize personal workload

· Self-organization

· Excellent communication skills

· Perform multiple tasks under minimum supervision

· Can do-attitude; enables change

· PRIVACY NOTICE:  To review the California privacy notice, click here:  https://agendia.com/privacy-policy/ 

· Employees must not be classified as an excluded individual who is prohibited from participation in any Federal health care program.

WORKING ENVIRONMENT

Establishes ADA (Americans with Disabilities Act) requirements

ENVIRONMENT/SAFETY/WORK CONDITIONS

Working conditions (inside or outside the office).

· Regularly walks, stands, and sits

· Ability to lift 30 pounds unassisted

· Regularly works on a computer for approximately 6-8 hours a day

· May be traveling plan, train, car, etc. for extensive amounts of time

TRAVEL

· Ability to travel to meet territorial requirements of up to 75%

OTHER DUTIES

Other duties as required by management

About the company

Agendia Inc.

Agendia, a precision oncology company, helps physicians and patients make personalized treatment decisions in early-stage breast cancer. MammaPrint® (MP), 70-gene breast cancer recurrence assay, is the only FDA-cleared (microarray) risk of recurrence test and is CE marked (IVDR-certified). BluePrint®(BP), 80-gene molecular subtyping assay, evaluates the underlying biology of a tumor to determine growth drivers. MP+BP are commercially available genomic tests, supported by clinical, guideline, peer-reviewed, and real-world evidence. They can be ordered on core biopsies or surgical specimens.*
*FDA Intended Use: the test is performed for breast cancer patients with Stage I or Stage II disease with tumor size ≤5.0cm and lymph node negative. The MP FFPE result is indicated for use by physicians as a prognostic marker only, along with other clinicopathological factors. Coverage criteria for majority of US health plans include early-stage breast cancer, tumor size less than or equal to 5.0cm (≤5.0cm), up to 3 positive lymph nodes, independent of receptor status, as validated in the 6,693 patient MINDACT trial. IVDR-CE mark Intended Use: you are a female breast cancer patient with Stage I or Stage II disease who is lymph node negative or lymph node positive with up to 3 positive nodes and for patients with stage III disease. The MP FFPE result is indicated for use by physicians and should be interpreted with other clinico-pathological factors. BP was developed and its performance characteristics determined by Agendia. It has not been cleared or approved by the US FDA, which determined that such clearance or approval is not necessary. This test is used for clinical purposes. It should not be regarded as investigational or for research. This test was performed at Agendia, Inc (05D1089250), which is certified under CLIA as qualified to perform high-complexity clinical laboratory testing. It is CE-marked for use in Europe. Social media policy: agendia.com/legal-compliance

Founded

2003

Company size

51-200 employees

Industry

Biotechnology

Org type

Privately Held

Headquarters

Irvine, CA

Apply Now

About the company

Agendia Inc.

Agendia, a precision oncology company, helps physicians and patients make personalized treatment decisions in early-stage breast cancer. MammaPrint® (MP), 70-gene breast cancer recurrence assay, is the only FDA-cleared (microarray) risk of recurrence test and is CE marked (IVDR-certified). BluePrint®(BP), 80-gene molecular subtyping assay, evaluates the underlying biology of a tumor to determine growth drivers. MP+BP are commercially available genomic tests, supported by clinical, guideline, peer-reviewed, and real-world evidence. They can be ordered on core biopsies or surgical specimens.*
*FDA Intended Use: the test is performed for breast cancer patients with Stage I or Stage II disease with tumor size ≤5.0cm and lymph node negative. The MP FFPE result is indicated for use by physicians as a prognostic marker only, along with other clinicopathological factors. Coverage criteria for majority of US health plans include early-stage breast cancer, tumor size less than or equal to 5.0cm (≤5.0cm), up to 3 positive lymph nodes, independent of receptor status, as validated in the 6,693 patient MINDACT trial. IVDR-CE mark Intended Use: you are a female breast cancer patient with Stage I or Stage II disease who is lymph node negative or lymph node positive with up to 3 positive nodes and for patients with stage III disease. The MP FFPE result is indicated for use by physicians and should be interpreted with other clinico-pathological factors. BP was developed and its performance characteristics determined by Agendia. It has not been cleared or approved by the US FDA, which determined that such clearance or approval is not necessary. This test is used for clinical purposes. It should not be regarded as investigational or for research. This test was performed at Agendia, Inc (05D1089250), which is certified under CLIA as qualified to perform high-complexity clinical laboratory testing. It is CE-marked for use in Europe. Social media policy: agendia.com/legal-compliance

Founded

2003

Company size

51-200 employees

Industry

Biotechnology

Org type

Privately Held

Headquarters

Irvine, CA

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