Career Opportunity

Marketing Communications – US

Life Molecular Imaging (LMI) is a global, innovative company focusing on the development and commercialization of molecular imaging radiopharmaceuticals for our approved F-18 amyloid PET tracer Neuraceq® and a pipeline of PET tracers in clinical development. LMI continues to grow at a steady pace creating the need for the following full-time position:

Marketing Communications - US

Marketing Communications (Marcom) will be responsible for the development and execution of the tactical elements of the North American Neuraceq® brand strategy, digital marketing campaign, social media platform, and responsible for the communication plans to support Life Molecular Imaging pipeline compounds. The US team is 100% home-based, but you will be required to travel up to 25% of the time This position will work with other team members across the US and Globally and therefore, you must be flexible to work outside the normal business hours when needed to support other time zones.  This position would ideally be located in the Eastern or Central Time Zones.

Key Tasks and Responsibilities:

  • Develop and implement US tactical plan with corresponding PR (including advocate and medical society plans) and programs aligned to support US brand strategy.
  • Build, implement, operate, and maintain a digital media & marketing strategy & platform with associated analytics to grow presence in associated markets.
  • Work with internal and external sources in the development, production, and timely distribution of marketing materials for field teams.
  • Ensure all marketing collateral has been approved by the Internal Review Committee (IRC).
  • Work closely with Sales and Medical Affairs on the training and rollout of marketing materials. This includes live training, as well as the development of implementation-guides and/or SOP for all pieces and programs rolled out to the field.
  • Accountable for managing assigned elements of US marketing budget. This includes the development of Statement of Work and corresponding contract request forms, timely submission of invoices, and budget reconciliations per project.
  • Support planning and execution of US regional and national congresses and tradeshows.
  • Liaise with Corporate PR on the approval of all press releases and ensure releases are uploaded to company website and sent to all LMI team members.

What we expect:
To be successful in this role, you will have proven experience in superior interpersonal and verbal/written communication skills. Have an established track record of experience in building and leading a digital marketing campaign for brand awareness. Advanced knowledge of Microsoft Office products and other marketing software. Bachelor’s degree in relevant field and three-five years of work experience in a biopharma or brand marketing role. Further direct experience will be considered in lieu of education. Ability to prioritize tasks and meet goals within deadlines. We are looking for people who are just as passionate as we are to improving the lives of those with Alzheimer’s and other neurodegenerative diseases and are excited to work for a growing company.

What you can expect:
LMI will provide the technology and training needed along with the support of coworkers, managers, and other divisions of the company.  You will be able to make significant contributions through your expertise. You can expect what YOU do to matter. All our employees are an integral part of a global organization, as well as the people and communities we serve.

Life Molecular Imaging, Inc. is an Equal Opportunity Employer. We believe what we do and our culture of “More Than a Job. It’s Making Life Better” extends to creating a welcoming, safe, and inclusive work environment.   If you have what it takes and the passion to make a difference, please visit our website to learn more. www.life-mi.com

Please send any inquiries, or submit cover letter with resume to: hr.us@life-mi.com

Neuraceq® - Product Indications And Use

PRODUCT INDICATIONS AND USE: Neuraceq is indicated for Positron Emission Tomography (PET) imaging of the brain to estimate β-amyloid neuritic plaque density in adult patients with cognitive impairment who are being evaluated for Alzheimer’s Disease (AD) and other causes of cognitive decline. A negative Neuraceq scan indicates sparse to no neuritic plaques and is inconsistent with a neuropathological diagnosis of AD at the time of image acquisition; a negative scan result reduces the likelihood that a patient’s cognitive impairment is due to AD. A positive Neuraceq scan indicates moderate to frequent amyloid neuritic plaques; neuropathological examination has shown this amount of amyloid neuritic plaque is present in patients with AD, but may also be present in patients with other types of neurologic conditions as well as older people with normal cognition. Neuraceq is an adjunct to other diagnostic evaluations.

Limitations: Limitations of Use
A positive Neuraceq scan does not establish the diagnosis of AD or any other cognitive disorder. The safety and effectiveness of Neuraceq have not been established for Predicting the development of dementia or other neurologic conditions or monitoring responses to therapies.

IMPORTANT SAFETY INFORMATION
CONTRAINDICATIONS: None

WARNINGS AND PRECAUTIONS

  • Risk for Image Misinterpretation and other Errors
    Errors may occur in the Neuraceq estimation of brain neuritic β-amyloid plaque density during image interpretation [see Clinical Studies (14)]. Image interpretation should be performed independently of the patient’s clinical information. The use of clinical information in the interpretation of Neuraceq images has not been evaluated and may lead to errors. Errors may also occur in cases with severe brain atrophy that limits the ability to distinguish gray and white matter on the Neuraceq scan. Errors may also occur due to motion artifacts that result in image distortion. Neuraceq scan results are indicative of the presence of brain neuritic β-amyloid plaques only at the time of image acquisition and a negative scan result does not preclude the development of brain neuritic β-amyloid plaques in the future.
  • Radiation Risk
    Neuraceq, similar to other radiopharmaceuticals, contributes to a patient's overall long-term cumulative radiation exposure. Long-term cumulative radiation exposure is associated with an increased risk of cancer. Ensure safe handling to protect patients and health care workers from unintentional radiation exposure [see Dosage and Administration.

ADVERSE REACTIONS:

  • The most commonly reported adverse reactions in clinical trials were injection site pain (3.4%), injection/appliucation site erythema (1.7%), injection site irritation (1.1%).

DRUG INTERACTIONS

  • Drug-drug interaction studies have not been performed in patients to establish the extent, if any, to which concomitant medications may alter Neuraceq image results.

USE IN SPECIFIC POPULATIONS

  • Pregnancy: All radiopharmaceuticals, including Neuraceq, have a potential to cause fetal harm depending on the stage of fetal development and the magnitude of the radiopharmaceutical dose. If considering Neuraceq administration to a pregnant woman, inform the patient about the potential for adverse pregnancy outcomes based on the radiation dose from the drug and the gestational timing of exposure.
  • Lactation: There are no data on the presence of florbetaben F 18 injection in human milk, the effects on the breastfed infant, or the effects of florbetaben F 18 injection on milk production. Exposure of Neuraceq to a breastfed infant can be minimized by temporary discontinuation of breastfeeding. The developmental and health benefits of breastfeeding should be considered along with the mother's clinical need for Neuraceq and any potential adverse effects on the breastfed child from Neuraceq or from the underlying maternal condition.
  • Pediatric Use: Neuraceq is not indicated for use in pediatric patients.
  • Geriatric Use: No overall differences in safety were observed between older and younger subjects

OVERDOSAGE
A pharmacological overdose of Neuraceq is unlikely given the relatively low doses used for diagnostic purposes. In the event of administration of a radiation overdose with Neuraceq, the absorbed organ dose to the patient should be reduced by increasing elimination of the radionuclide from the body by inducing frequent micturition. Prior to Neuraceq administration, please read the full Prescribing Information for additional Important Safety Information.

SUSPECTED ADVERSE REACTIONS please report to: https://www.fda.gov/safety/medwatch-fda-safety-information-and-adverse-event-reporting-program

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