ARTO

Business Development Manager

Massachusetts, US

16 days ago
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Summary

Job Summary:

We are seeking a dynamic and results-driven Business Development Manager to join our team and drive the growth of our small molecule CDMO services. The ideal candidate will have a strong understanding of pharmaceutical development and manufacturing processes, combined with a strategic sales mindset. This role will be responsible for identifying new business opportunities, building relationships with clients, and expanding our customer base in the pharmaceutical and biotech sectors.


Key Responsibilities:

  • Identify and pursue new business opportunities within the small molecule development and manufacturing space.
  • Develop and maintain strong relationships with pharmaceutical and biotech clients.
  • Lead the end-to-end sales process, including prospecting, proposal development, contract negotiations, and closing deals.
  • Collaborate with internal teams (R&D, manufacturing, regulatory, project management) to ensure alignment of technical capabilities with client needs.
  • Attend industry conferences, networking events, and trade shows to represent the company and generate leads.
  • Monitor market trends, competitor activities, and customer feedback to inform strategic planning.
  • Maintain accurate records of sales activities and pipeline status using CRM tools.
  • Prepare and present regular business reports, forecasts, and strategic plans to senior management.


Qualifications:

  • Bachelor’s or Master’s degree in Chemistry, Pharmaceutical Sciences, Life Sciences, or related field.
  • Minimum 5 years of experience in business development or sales, ideally within a CDMO or pharmaceutical services environment.
  • Strong knowledge of small molecule drug development and manufacturing processes (e.g., API synthesis, formulation, analytical services).
  • Excellent communication, negotiation, and interpersonal skills.
  • Proven track record of meeting or exceeding sales targets.
  • Ability to work independently and manage multiple priorities in a fast-paced environment.
  • Willingness to travel as needed (~30–50%).


Preferred Qualifications:

  • Experience working with both early-phase and commercial-scale clients.
  • Familiarity with GMP manufacturing and regulatory requirements.
  • Existing network of industry contacts in pharma and biotech.

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