Business Development Director – Overseas

Allsino Pharmaceutical Co., Ltd.

Boston (MA)

In loco

USD 150.000 - 230.000

Tempo pieno

14 giorni+
Generatore di candidature

Una candidatura completa in un minuto — curriculum e lettera di presentazione personalizzati, pronti da inviare.

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Descrizione del lavoro

Allsino Pharmaceutical Co., Ltd. in Boston is seeking a senior business development leader to direct BD activities and drive sales growth. You will play a key role in the company and in generating new business, while also managing marketing and customer service initiatives.

The position requires extensive CDMO BD experience in US/EU markets, strong negotiation skills, and deep knowledge of drug development and regulatory frameworks. Travel across the US and Europe is expected.

Competenze

  • Master's or PhD in Organic Chemistry, Pharmaceutical Sciences, or related life science fields.
  • CDMO business development experience in US/EU markets with successful track record in small molecule, peptide, and API project acquisition.
  • Strong C-level negotiation and cross-cultural communication skills.
  • Solid knowledge of drug development, API/intermediate manufacturing, and global CDMO regulatory frameworks.
  • Fluent in English; additional European languages are a plus.
  • Willingness to travel frequently across the US and Europe.

Mansioni

  • Drive CDMO business development in US/EU markets for small molecules, peptides, and APIs—identify client needs and secure R&D/manufacturing projects.
  • Lead high-level negotiations with pharma companies and research institutes to finalize agreements and ensure smooth project execution.
  • Expand networks with key decision-makers in the European and US pharmaceutical industries, building a sustainable CDMO project pipeline.
  • Develop business proposals including financial analysis, risk assessment, and market strategies for senior management review.
  • Oversee contract drafting, review, and execution in compliance with international regulations and company policies.
  • Maintain long-term global client relationships, track project progress, and optimize strategies to meet sales and growth targets.
  • Monitor industry trends, regulatory updates, and competitor activities to support strategic planning.

Conoscenze

Negotiation
Cross-cultural communication
Pharma business development

Formazione

Master's/PhD in Organic Chemistry or Pharmaceutical Sciences

Descrizione del lavoro

The ideal candidate will direct the business development activities of the organization and drive the sales business. They play a key role in the company and in the generation of new business. This individual will also be responsible for managing marketing and customer service activities.

Responsibilities
  • Drive CDMO business development in US/EU markets for small molecules, peptides, and APIs—identify client needs and secure R&D/manufacturing projects.
  • Lead high-level negotiations with pharma companies and research institutes to finalize agreements and ensure smooth project execution.
  • Expand networks with key decision-makers in the European and US pharmaceutical industries, building a sustainable CDMO project pipeline.
  • Develop business proposals including financial analysis, risk assessment, and market strategies for senior management review.
  • Oversee contract drafting, review, and execution in compliance with international regulations and company policies.
  • Maintain long-term global client relationships, track project progress, and optimize strategies to meet sales and growth targets.
  • Monitor industry trends, regulatory updates, and competitor activities to support strategic planning.
Qualifications
  • Master's or PhD in Organic Chemistry, Pharmaceutical Sciences, or related life science fields.
  • Proven CDMO business development experience in US/EU markets with successful track record in small molecule, peptide, and API project acquisition.
  • Strong C-level negotiation and cross-cultural communication skills.
  • Solid knowledge of drug development, API/intermediate manufacturing, and global CDMO regulatory frameworks.
  • Fluent in English; additional European languages are a plus.
  • Willingness to travel frequently across the US and Europe.
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