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Crp-Global Med Affairs, Nbu, Substance Use Disorders

0-2 years
$198,000 to $336,600.
10 March 24, 2025
Job Description
Job Type: Full Time Education: MD/DO Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 


CRP-Global Med Affairs, NBU, Substance Use Disorders
Location: Indianapolis, Indiana, United States
Category: Medical
Job Type: Full Time, Regular
Job Id: R-76896

Purpose:
The Clinical Research Physician (CRP) in the Neuroscience Business Unit – Medical Affairs applies scientific and medical expertise to strategic planning, launch, and commercialization efforts. They ensure alignment with business unit priorities and global teams to address customer needs. The CRP engages with providers, patients, and payers while supporting global Development, Clinical Pharmacology, and Translational Medicine activities across all clinical trial phases. They ensure compliance with local and international regulations while enhancing the customer experience.

Primary Responsibilities:

1. Business/Customer Support (Pre and Post Launch):

  • Understand and address scientific information needs of customers (payers, patients, HCPs).

  • Develop and implement medical strategies for brand commercialization.

  • Support pricing, reimbursement, and access (PRA) plans.

  • Lead local scientific data dissemination through conferences and advisory boards.

  • Contribute to the development and approval of promotional materials.

  • Train sales and medical representatives.

  • Define the patient journey and advocate for patient needs.

2. Scientific Data Dissemination/Exchange:

  • Ensure compliance with local laws and global policies in data dissemination.

  • Address unsolicited scientific queries from healthcare professionals.

  • Plan and lead symposia, advisory board meetings, and scientific programs.

  • Develop and review scientific content for educational materials.

  • Build and maintain relationships with external scientific experts and professional societies.

3. Clinical Planning:

  • Collaborate with global teams to ensure clinical plans meet local/regional customer needs.

  • Represent local/regional clinical needs to business unit medical leadership.

  • Maintain knowledge of pre-clinical and clinical data relevant to the molecule.

4. Clinical Research/Trial Execution and Support:

  • Approve informed consent documents and risk profiles.

  • Assist in protocol development, investigator selection, and study startup activities.

  • Monitor patient safety and address site/investigator questions during study conduct.

5. Regulatory Support Activities:

  • Support local labeling, registration efforts, and communication with regulatory agencies.

  • Participate in risk management planning and regulatory advisory committees.

6. Scientific/Technical Expertise and Development:

  • Stay current with trends in clinical practice and competitive product data.

  • Provide scientific training and consultation to the clinical study team.

  • Attend and contribute to medical congresses and scientific symposia.

7. General Responsibilities:

  • Support business unit management in administering medical budgets.

  • Set professional development goals and provide coaching/feedback to co-workers.

  • Collaborate effectively with internal teams and external partners.

Compensation:
Actual compensation depends on education, experience, skills, and location. The anticipated wage for this position ranges from $198,000 to $336,600.