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Eli Lilly and Company

Alliance Diabetes & Obesity CRP

Basingstoke
Posted about 19 hours ago
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Business/Customer Support

  • Understand and anticipate the scientific information needs of all local/regional customers (payers, patients, healthcare providers) and actively address their questions in a timely fashion by leading data analyses and new clinical or health outcomes research efforts.
  • Contribute to the development of medical strategies to support brand commercialization activities by working closely with the global Medical Affairs and brand teams, Global Patient Outcomes/Real World Evidence and global PRA, clinical management or personnel, and other cross-functional management during the development of the local business plan.

Scientific Data Dissemination/Exchange

  • Knowledge of and compliance with local laws and regulations, and global policies and procedures, compliance guidelines with respect to data dissemination and interactions with external healthcare professionals.
  • Understand and actively address the unsolicited scientific information needs of external healthcare professionals according to guidelines above.
  • Support medical information associates in preparation and review of medical letters and other medical information materials.
  • Establish and maintain appropriate collaborations and relationships with external scientific experts, thought leaders, and the general medical community on a local, national, regional, and possibly international basis.

Clinical Planning & Clinical Research/Trial Execution and Support

Reasons to use Rodeo

I’m in my final year doing Economics and I don’t know whether to apply for grad schemes now or do a masters first. What do you think?

Honest answer — it depends on where you want to end up. A lot of top grad schemes (Big 4, civil service, banking) don’t need a masters. Let’s look at the ones you’d be competitive for now, and we can decide if a masters actually adds anything.

Also worth knowing: most autumn 2026 applications are open now. Timing matters more than you think.

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Graduate Consultant — 2026 Scheme

PwC·London, UK
£35,000/yr

Why you're a good match

Strong

Your economics background and your summer at a regional bank line up with what PwC looks for on the consulting scheme. Applications close in four weeks.

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It searches the market for you

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Why you're a good match

You’ve got the grades and the economics background, and your bank internship is exactly the experience this scheme looks for. Apply soon — deadlines close within the month.

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Strong

Experience fit

Your summer at the bank plus your econometrics coursework map directly to the day-one responsibilities on this scheme — client modelling, market briefings, and deal support.

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Strong

Only hits

No noise. No "maybe this fits." Just roles with a clear explanation of why they're right — and where to focus when applying.

  • Represent 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.
  • Review and approve local informed consent documents and risk profiles to ensure appropriate communication of risk to study subjects.
  • Collaborate with clinical research staff in the design, conduct, and reporting of local clinical trials (for example, sample size, patient commitment, timelines, grants, and governance review interactions) - Whenever necessary.

Regulatory Support Activities

  • Participate in development and review of local labelling and labelling modifications in collaboration with global Development, brand teams, regulatory, and legal. Demonstrate deep knowledge of local label.
  • Provide medical expertise to regulatory scientists.
  • Participate in advisory committees.

Scientific Technical Expertise

  • Be aware of current trends and projections for clinical practice and access in the therapeutic area(s) relevant to the product, both near term (1-2 years) and longer-term (3-5 years).
  • Critically read and evaluate the relevant medical literature; know the status and data from competitive products; and keep updated with medical and other scientific developments relevant to the product.
  • Acts as scientific consultant and protocol expert for clinical study team members and others in medical.

Qualifications

  • Medical Doctor or Doctor of Osteopathy. Must be board eligible or certified in the appropriate specialty/subspecialty or have completed the comparable level of post-medical school clinical training relevant to the country of hiring.
  • Must have completed education and training at a medical school that meets the requirements of the Liaison Committee on Medical Education.
  • Fluent in English, both verbal and written communication.
  • Knowledge of drug development process relevant to country/region preferred.
  • Strong communication, organizational, and negotiation skills.
  • Demonstrated ability to influence others to create a positive working environment.

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Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

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.

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Location

Basingstoke, England, United Kingdom

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