Associate Director

Job not on LinkedIn

🔥 16 hours ago

🏈 Alabama, Florida, +4 more states – Remote

🏈 Alabama – Remote 🐊 Florida – Remote ⚜️ Louisiana – Remote 🎸 Mississippi – Remote 🌴 South Carolina – Remote 🎸 Tennessee – Remote

💵 $156k - $250.8k / year

⏰ Full Time

🟠 Senior

👔 Director

👻 Ghost score 0%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Eli Lilly and Company

WebsiteLinkedInAll Job Openings

10,000+ employees

💊 Pharmaceuticals

🏥 Healthcare

🧬 Biotechnology

💰 $6.5M Post-IPO Debt - Eli Lilly on 2024-02

Pharmaceuticals • Healthcare • Biotechnology

Eli Lilly and Company is a multinational pharmaceutical company that researches, develops, manufactures, and markets prescription medicines across multiple therapeutic areas including diabetes, oncology, immunology, neuroscience, and pain. Headquartered in Indianapolis, Indiana, Lilly is known for its extensive R&D, clinical development, and global commercialization of biologic and small-molecule drugs. The company focuses on drug discovery, clinical trials, regulatory approvals, and large-scale pharmaceutical manufacturing and distribution.

📋 Description

• Serve as a field-based scientific expert engaging healthcare professionals and supporting clinical development • Translate complex scientific data into meaningful clinical insights and foster compliant, evidence-based dialogue with thought leaders • Maintain therapeutic-area expertise and scientific knowledge relevant to Centessa’s pipeline and marketed products • Engage in compliant, non-promotional scientific exchange with KOLs, investigators, and other HCPs • Provide accurate and balanced medical information to external stakeholders • Deliver company-approved medical/scientific presentations to formulary committees and healthcare professionals • Support speaker training, advisory boards, and sales training as appropriate • Document field-based activities accurately, timely, and compliantly • Collaborate with Clinical Operations to identify and evaluate clinical trial sites and investigators • Provide scientific education and protocol-specific training during site initiation visits • Maintain engagement with trial sites and investigators to support trial execution, address protocol inquiries, and ensure high-quality data generation • Attend scientific and medical congresses and provide insights and post-conference reports • Support congress activities through pre-conference plans, booth coverage, symposia participation, and KOL engagement • Contribute to scientific slide decks, FAQs, and educational materials • Write and edit Medical Information response letters • Ensure materials are medically accurate, evidence-based, and compliant with regulatory standards • Collaborate with Medical Affairs and Legal teams on scientific content • Lead MSL strategic initiatives and projects • Develop and implement scientific training plans for the MSL team • Mentor MSL peers

🎯 Requirements

• Advanced degree (PhD, PharmD, MD) in life sciences or a related field from an accredited college or university • Minimum of 2 years of experience in a Medical Affairs or MSL role within the pharmaceutical or biotech industry • Excellent understanding of sleep medicine and associated therapeutic areas strongly preferred • Exceptional verbal and written communication skills • Ability to tailor scientific messages to diverse audiences • Ability to interpret and communicate complex scientific data • Proven ability to build and maintain strong relationships with KOLs, investigators, and internal stakeholders • Strong understanding of clinical trial design, regulatory requirements, and therapeutic area landscape • Skilled in developing and delivering scientific presentations in various settings • Strong understanding of industry regulations and guidelines governing medical interactions • Ability to align field activities with broader medical and corporate strategies • Must have a valid driver’s license with a driving record that meets company requirements • Willing and able to travel frequently throughout the Southeast region, including Alabama, Arkansas, Florida, Georgia, Louisiana, Mississippi, South Carolina, and Tennessee • Must reside in the Atlanta metropolitan area or a major Florida metropolitan area with access to a major commercial airport

🏖️ Benefits

• Company bonus depending, in part, on company and individual performance • Company-sponsored 401(k) • Pension • Vacation benefits • Medical benefits • Dental benefits • Vision benefits • Prescription drug benefits • Flexible benefits, including healthcare and/or dependent day care flexible spending accounts • Life insurance and death benefits • Time off and leave of absence benefits • Well-being benefits, including employee assistance program, fitness benefits, and employee clubs and activities