Clinical Research Scientist – Neuroscience

2 months ago

Sydney, Australia Lilly Full time

We’re looking for people who are determined to make life better for people around the world.

Clinical Research Scientist – Neuroscience

Purpose:
 

Through the application of scientific and clinical training and expertise, the Clinical Research Scientist (CRS) is an integral member of the medical affairs, development or a business unit brand team for strategic planning in the support of launch and commercialization activities to meet patients' needs and ultimately enhance the customers' experience in interacting with the company.

Primary Responsibilities :

Business/ customer support (pre and post launch support)Understand and anticipate the scientific information needs of all local/regional customersContribute to the development of medical strategies to support brand commercializationContribute as a scientific and clinical expertSupport business-to-business and business-to-government activitiesContribute actively on an ongoing basis to the strategic planning for currently marketed brandsSupport training of sales representatives, and other medical representativesParticipate in local or national trade associations as appropriate.
  Scientific Data Dissemination/ExchangeKnowledge of and compliance with local laws and regulations, and global policies and procedures, compliance guidelines with respect to data dissemination and interactions with external health care professionalsUnderstand and actively address the unsolicited scientific information needs of external health care professionals according to guidelines aboveSupport the planning of symposia, advisory board meetingsPrepare or review scientific information in response to customer questions or media requestsProvide congress supportParticipate in data analysesParticipate in reporting of clinical trial data in Clinical Trial Registry activities.
  Clinical PlanningCommunicate and collaborate with Director-Medical and Business Unit Team Physician/Regional Medical Leader as needed to ensure life cycle plans for drugs in development address customer needsCommunicate local/regional research needs and collaborate with other regions and the global Development and Medical Affairs teamsUnderstand and keep updated with the pre-clinical and clinical data relevant to the moleculeRepresent the clinical needs of the country/region to the business unit medical leadership in the development of clinical strategies, development plans and study protocol design.
  Clinical Research/Trial Execution and SupportReview and approve local informed consent documents and risk profiles to ensure appropriate communication of risk to study subjectsCollaborate with clinical research staff in the design, conduct and reporting of local clinical trialsCollaborate with clinical research staff, regional clinical operations staff, statisticians, global patient outcomes, research scientists and selected investigators in the development of protocols and data collection requirementsParticipate in investigator identification and selection, in conjunction with clinical teamsAssist in the planning process and participate in study start-up meetings and other activities to provide the appropriate scientific training and information to investigators and site personnelServe as resource to clinical research site monitors, investigators and ethical review boards.
  General ResponsibilitiesSupport the business unit management team, including medical leadership in preparation and administration of the local or business unit medical budgetCollaborate proactively and productively with all alliance, business, and vendor partnersAs applicable, works closely with direct reports on performance management plans (objectives), development plansActively participate in recruitment, diversity, and retention and hiring efforts

Launch Readiness Planning

The medical launch leader is responsible for the strategy, planning and execution of those medical activities that will complement registration studies in achieving successful product launches and increasing benefits to patients. Collaborate with global brand development teams, Business Unit Team Physician/Regional Medical leader, and local cross-functional team members for launch preparations.Insights, patient segmentation, competitive landscapeLocal position, brand planningLocal commercialization activitiesResponsible for launch readiness capabilityResponsible to lead and drive competition of the Medical Affairs launch readiness activities

Minimum Qualification Requirements:

An advanced health/medical/scientific (for example, in Pharmacology, physiology, microbiology) or related graduate degree such as DVM, PharmD, PhD, MSN with advanced clinical specialty (Clinical Nurse Specialist/Nurse Practitioner) and one of following
 

3-5 years of clinical experience or 3-5 years of pharmaceutical experience (2 of which is in clinical development)
 

OR

Have a BS or Masters degree in health/medical/scientific or related field and 7-10 years of pharmaceutical experience that is directly related to at least one of the following
 

Clinical trial experience

Experience in areas relevant to drug discovery

Drug/clinical development experience (for example, epidemiology, toxicology, pharmacology, regulatory affairs, medical affairs)

Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.

#WeAreLilly

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