Eli Lilly and Company

Director – Clinical Research Scientist

Eli Lilly and Company

full-time

Posted on:

Location Type: Office

Location: IndianapolisUnited States

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Salary

💰 $151,500 - $259,600 per year

Job Level

About the role

  • contribute to the oversight of clinical development program(s) in support of overall clinical development strategy and vision
  • serve as liaison and resource to various physicians and clinical trial sites
  • apply scientific and clinical training and expertise to described roles
  • support the build, analysis, interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study reports, regulatory submissions and responses, publications and data dissemination for products
  • ensure adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality standards in conducting research
  • engage in clinical development contributions to due diligence or other business development activity
  • design and implement translational strategies in collaboration with research colleagues
  • solicit opinion leader interactions related to the disease area(s)
  • stay abreast of professional information and technology through conferences, medical literature, and other available training
  • to augment expertise in the therapeutic area

Requirements

  • An advanced health/medical/scientific degree (such as DVM, PharmD, PhD, or MSN with advanced clinical specialty)
  • 1+ years Clinical Trials/Research experience in pharmaceutical industry, academia, research setting
  • strong preference for experience within in Oncology and/or Hematology
  • Breast cancer disease area knowledge
  • Ability to develop collaborative working relationships with physicians, expert consultants, and contracted vendors
  • Strong analytical mind and problem-solving skills
  • Thoughtful detail, strong organizational skills, and ability to work independently within a team
  • Proven track record to bring out the best in others on a cross-functional international team
  • Leading by influence
  • Strong documentation and leadership qualities, including proficiency with MS Word, EndNote, PowerPoint and Excel
  • Strong communication, both written and oral
  • Ability to multi-task and shift priorities rapidly to meet target dates.
Benefits
  • eligibility to participate in a company-sponsored 401(k)
  • pension
  • vacation benefits
  • eligibility for medical, dental, vision and prescription drug benefits
  • flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts)
  • life insurance and death benefits
  • certain time off and leave of absence benefits
  • well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities)
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
clinical trialsresearchdata analysisprotocol developmentregulatory submissionsscientific reportingpharmacovigilancetranslational strategiesoncologyhematology
Soft Skills
collaborative working relationshipsanalytical skillsproblem-solvingorganizational skillsindependent workteamworkleadershipcommunication skillsmulti-taskingadaptability
Certifications
DVMPharmDPhDMSN