Full-Time

Director – Business Development

ProPharma Group

ProPharma Group

1,001-5,000 employees

Regulatory sciences consultant for life sciences

No salary listed

Remote in USA

Remote

Remote within the United States.

Category
Business & Strategy (1)
Required Skills
Market Research
Sales
Lead Generation
Marketing

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Requirements
  • Bachelor’s degree in a related field
  • At least 5 years of sales or recruiting experience within the life sciences field.
  • Proven team builder and team player who can focus and continuously reinforce efforts to meet goals.
  • Strong presence and confidence during presentations to customers.
  • Exceptional time management skills.
  • Excellent analytical skills and the ability to assess and resolve difficult business situations.
  • A problem solver – analyzing and problem resolution at both a strategic and functional level.
  • High level of ambition, resilient and flexible – able to deal with ambiguity and change, within a midsize but high-growth business.
  • A self-starter with a driving personality and willingness to take on responsibilities in a proactive manner.
Responsibilities
  • Develop and maintain long-term client relationships resulting in the expansion of our client base, build awareness of our company services and generate revenue.
  • Uncover immediate needs to target market through leads and follow ups, executing internal and external initiatives to drive profitable growth.
  • Support direct sales initiative by creating and participating in sales meetings and presentations.
  • Identify and attend key conferences and trade shows to increase company visibility and business opportunities.
  • Negotiate contracts and agreements.
  • Generate new leads and opportunities.
  • Develop and write proposals for submission to prospective clients.
  • Initiate and facilitate pre-work with a client as needed (e.g. CDA/NDA, MSA, SOW, meeting preparations).
  • Act as a liaison between ProPharma and potential clients (e.g., setting up capability presentations, teleconference).
  • Document leads, opportunities, proposals, and related activities in CRM.
  • Liaise with client during proposal negotiation.
  • Work closely with client-facing teams outside of the Business Development function on sales strategies based on market research and competitor analyses and execute sales plan based on those strategies.
  • Conduct sales follow-up and order close with prospective customers.
  • Work with Marketing to coordinate promotions, participate in events, and conduct follow-up contact with prospective clients.
  • Utilize internal data tracking tools to record and monitor ongoing sales activities and for producing sales metrics reports as needed.
  • Ensure communications are coordinated with internal stakeholders, and support sales plan objectives.
  • Participate in regular Business Development team meetings and meetings with key stakeholders.
  • Other duties as assigned.

ProPharma Group provides regulatory sciences consulting and related services for drugs, biologics, medical devices, and diagnostics on a global scale. Its offerings cover the full lifecycle, from early development and clinical trials to regulatory approval and post-market activities. The company’s services include regulatory sciences, clinical research, quality and compliance, pharmacovigilance, medical information, and R&D technology, delivered by a team of over 2,500 professionals with more than 20 years of operation. ProPharma Group differentiates itself by providing expert, end-to-end regulatory and life sciences solutions across multiple product types and stages, helping pharmaceutical, biotechnology, and medical device companies navigate complex regulatory and compliance challenges. The goal is to help clients bring safe and compliant products to market efficiently while maintaining ongoing lifecycle support.

Company Size

1,001-5,000

Company Stage

N/A

Total Funding

N/A

Headquarters

Raleigh, North Carolina

Founded

2001

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Simplify Jobs

Simplify's Take

What believers are saying

  • July 8, 2026 AI capability shortens ANDA timelines and lowers manual authoring costs.
  • May 27, 2026 Adrian Pencak strengthens global commercial execution across life sciences.
  • December 2025 Hyderabad office expands capacity and improves access to Indian talent.

What critics are saying

  • ProPharma's 2021 merger with The Planet Group complicates integration and management focus.
  • Private-equity ownership under Odyssey pressures margins, cross-sell, and exit readiness by 2027.
  • Big rivals like IQVIA and ICON can outspend ProPharma on technology and talent.

What makes ProPharma Group unique

  • July 2026 AI-assisted ANDA drafting speeds submissions without replacing regulatory experts.
  • June 2026 Kevin van Dooren adds integrated EU HEOR, HTA, and market access.
  • Hyderabad expansion and Odyssey backing support global delivery scale across regulated services.

Help us improve and share your feedback! Did you find this helpful?

Benefits

Remote Work Options

Growth & Insights and Company News

Headcount

6 month growth

0%

1 year growth

0%

2 year growth

24%
Compli
Aug 5th, 2026
Welcome Laurie Rouse and Todd Sevier to the Compli team.

Welcome Laurie Rouse and Todd Sevier to the Compli team. August 5, 2026 Compli is excited to welcome two new hires into its leadership team, even furthering its team's strength and operational success. Laurie Rouse joins its team as Operations Manager and Todd Sevier as Principal - (Commissioning, Qualification and Validation services (CQV). "I am excited to welcome Todd and Laurie to the Compli team," said Compli President Greg Spanel. "Each brings a unique and valuable set of skills that will help drive Compli's vision for the future. Their addition strengthens our ability to better serve both our employees and our clients, while supporting our continued growth and success." Laurie Rouse - Operations Manager. Laurie has extensive experience in operations management, process improvement and administrative leadership, recently serving as Senior Manager of Global Audit Coordination at ProPharma Group. In this role, she oversaw the day-to-day operations of the global audit department and partnered with cross-functional teams to develop and implement departmental processes and policies. "This is an exciting opportunity to join Compli at a time of continued growth. I look forward to contributing to operational improvements, supporting our talented team and helping the organization achieve its strategic objectives." said Rouse. In her new role, Laurie will help drive operational excellence, supporting strategic initiatives and positioning Compli for continued growth. Compli is excited to welcome Laurie to the team and look forward to the contributions she will make in the years ahead. Todd Sevier - Principal - CQV. Todd joined Compli most recently with ProPharma Group, where he served as Director of Compliance and Quality Assurance, bringing extensive experience in quality systems, regulatory compliance, validation, and project leadership within highly regulated industries. In his new role, Todd will lead Compli's CQV service group, providing strategic direction, technical expertise and mentorship to team members while supporting clients through CQV initiatives. His leadership will help strengthen Compli's commitment to delivering flexible, high-quality CQV solutions that support projects of all sizes and complexities. "I'm excited to join a team that is recognized for its technical expertise and client-focused approach," said Todd. "I look forward to working alongside the talented professionals at Compli, supporting our clients' success and helping grow the next generation of CQV leaders."

PR Newswire
Jul 8th, 2026
ProPharma deploys AI-assisted capability to accelerate ANDA submission development

ProPharma, a global provider of regulatory, clinical, and compliance services for life sciences, has launched a proprietary AI-assisted capability to enhance Abbreviated New Drug Application submission development. The technology, part of ProPharma's Technology Enablement Strategy, aggregates and analyses information from multiple data sources to generate structured first drafts, reducing manual authoring effort. The AI tool enables ProPharma's regulatory experts to focus on scientific evaluation, strategic guidance, and quality review. According to Matthew Weinberg, president of regulatory sciences, the capability aims to reduce authoring timelines whilst maintaining scientific rigour. Chief executive Dawn Sherman emphasised that the technology enhances rather than replaces expertise. ProPharma is integrating purpose-built technologies across its service areas, including regulatory affairs, clinical research, and pharmacovigilance. The company is a portfolio company of Odyssey Investment Partners.

Informa TechTarget
Jul 8th, 2026
ProPharma advances Technology Enablement Strategy with ai-assisted capability for ANDA submission development.

ProPharma advances Technology Enablement Strategy with ai-assisted capability for ANDA submission development. ProPharma's new proprietary tool accelerates regulatory submissions while ensuring top-tier quality and compliance for global pharmaceutical clients. July 8, 2026 Press Contacts Shannon Severino 412-608-2393 RALEIGH, N.C. - ProPharma, the leading global provider of regulatory, clinical, and compliance services for the life sciences industry and a portfolio company of Odyssey Investment Partners, today announced another milestone in its Technology Enablement Strategy with the deployment of a proprietary AI-assisted capability that enhances how the company develops Abbreviated New Drug Application (ANDA) submissions for clients. The AI-assisted capability was purpose-built to support ProPharma's regulatory teams and their clients in the development of ANDA submissions. By intelligently aggregating and analyzing information from multiple data sources and document formats, the technology generates structured first drafts that significantly reduce manual authoring effort. This enables ProPharma's regulatory experts to dedicate more time to scientific evaluation, strategic regulatory guidance, quality review, and client collaboration. "The future of regulatory submissions is not about replacing experts with technology," said Matthew Weinberg, President, Regulatory Sciences at ProPharma. "It's about empowering experts with better tools. By combining human expertise with AI-enabled efficiencies, we are helping clients reduce authoring timelines, improve operational effectiveness, and maintain the scientific rigor and regulatory excellence that have always been central to ProPharma's approach in a more cost-effective way." Developed specifically to enhance ProPharma's internal regulatory delivery process, the capability is designed to improve consistency, completeness, and traceability throughout submission development while supporting the rigorous quality and compliance standards expected by global health authorities. It also enables more efficient management of regulatory questions and deficiency responses throughout the submission lifecycle. For clients, these enhancements translate into meaningful benefits, including: * Accelerated ANDA preparation and submission timelines * Reduced manual document authoring effort * Improved consistency and completeness across submission content * Enhanced traceability throughout submission development * More efficient management of regulatory questions and deficiency responses * Better utilization of regulatory resources while maintaining high-quality submissions "Technology should enhance expertise, not replace it," said Dawn Sherman, Chief Executive Officer of ProPharma. "Our Technology Enablement Strategy reflects our commitment to continuously improving how we serve clients by equipping our experts with innovative capabilities that increase efficiency, strengthen quality, and accelerate delivery. This AI-assisted capability is one example of how we're investing in the future of expert-led life sciences services." Technology Enablement is ProPharma's enterprise-wide strategy for integrating proprietary technology, intelligent automation, and artificial intelligence into the way its experts deliver services across the organization. ProPharma is embedding purpose-built technologies into its expert-led delivery model across regulatory affairs, clinical research, pharmacovigilance, quality and compliance, medical information, and consulting services. The initiative is designed to improve efficiency, consistency, scalability, and client outcomes while preserving the scientific expertise, regulatory judgment, and human oversight that remain at the core of every engagement. For more than 25 years, ProPharma has improved patients' health and wellness by providing expert guidance that empowers biotech, pharmaceutical, and medical device organizations to confidently advance scientific breakthroughs and bring new therapies to market. With deep expertise in regulatory sciences, CRO services, quality and compliance, pharmacovigilance, medical information, FSP solutions, and digital transformation, ProPharma delivers integrated, end-to-end solutions that help organizations navigate complexity, mitigate risk, and accelerate the development and commercialization of life-changing therapies. For more information about ProPharma, please visit propharmagroup.com. Odyssey Investment Partners Odyssey Investment Partners is a leading private equity investment firm with more than a 25-year history of partnering with skilled managers to transform middle-market companies into more efficient and diversified businesses with strong growth profiles. Odyssey makes majority-controlled investments in industries with a long-term positive outlook and favorable secular trends. For further information about Odyssey, please visit odysseyinvestment.com.

Clinical Research News
May 27th, 2026
ProPharma appoints Adrian Pencak as Chief Commercial Officer.

ProPharma appoints Adrian Pencak as Chief Commercial Officer. May 27, 2026, 09:42 AM by Life Sciences Industry Veteran Appointed to Lead Global Commercial Organization RALEIGH, N.C. - May 27, 2026 - ProPharma, a leading provider of regulatory, clinical, and compliance services for the life sciences industry, today announced the appointment of Adrian Pencak as Chief Commercial Officer. He will be responsible for leading ProPharma's global commercial organization, across its full suite of regulatory, clinical, and compliance services. Pencak brings more than 25 years of executive commercial leadership experience across pharma services, clinical development, technology-enabled solutions, and global Contract Research Organizations. Throughout hiscareer, he has built and led high-performing commercial teams, driven significant global revenue growth, and developed scalable go-to-market strategies for many of the life sciences industry's leading organizations. Prior to joining ProPharma, he held senior commercial leadership positions at organizations including IQVIA, Advarra, PharmaLex, and ICON plc, where he focused on expanding strategic accounts, strengthening global partnerships, and advancing commercial growth across international markets. His experience spans both full-service outsourcing and Functional Service Provider (FSP) models, with a strong track record of supporting leading pharmaceutical, biotechnology, and life sciences organizations through complex development and commercialization initiatives. "Adrian brings deep commercial leadership experience across the life sciences services landscape and understands the importance of delivering integrated solutions that help clients navigate increasingly complex development and commercialization challenges," said Dawn Sherman, Chief Executive Officer of ProPharma. "His experience scaling global commercial organizations and building strong client partnerships will be an important asset as we continue expanding our global capabilities and supporting clients across the full product development lifecycle." "ProPharma has built an outstanding reputation for helping clients navigate complex regulatory, clinical, and compliance challenges across the product lifecycle to help bring therapies to patients faster," said Adrian Pencak. "I'm excited to join the organization at this stage of growth and look forward to partnering with teams across the business to strengthen strategic client relationships, scale commercial capabilities, and continue delivering high-value solutions that help accelerate innovation across the life sciences industry." Pencak is also active in the broader life sciences community as a speaker and contributor at industry events, including Bio-IT World and the European Clinical Data Forum. His work has included thought leadership on the use of technology and artificial intelligence in clinical and regulatory environments, as well as the modernization of pharma services operating models. About ProPharma For more than 25 years, ProPharma has improved patients' health and wellness by providing expert guidance that empowers biotech, pharmaceutical, and medical device organizations to confidently advance scientific breakthroughs and bring new therapies to market. With deep expertise in regulatory sciences, CRO services, quality and compliance, pharmacovigilance, medical information, FSP solutions, and digital transformation, ProPharma delivers integrated, end-to-end solutions that help organizations navigate complexity, mitigate risk, and accelerate the development and commercialization of life-changing therapies. For more information about ProPharma, please visit propharmagroup.com. About Odyssey Investment Partners Odyssey Investment Partners is a leading private equity investment firm with more than a 25-year history of partnering with skilled managers to transform middle-market companies into more efficient and diversified businesses with strong growth profiles. Odyssey makes majority-controlled investments in industries with a long-term positive outlook and favorable secular trends. For further information about Odyssey, please visit odysseyinvestment.com.

PR Newswire
May 27th, 2026
ProPharma appoints Adrian Pencak as chief commercial officer to lead global expansion

ProPharma, a provider of regulatory, clinical and compliance services for the life sciences industry, has appointed Adrian Pencak as Chief Commercial Officer. He will lead the company's global commercial organisation across its full service portfolio. Pencak brings over 25 years of executive commercial leadership experience in pharma services, clinical development and contract research organisations. He has previously held senior commercial positions at IQVIA, Advarra, PharmaLex and ICON plc, focusing on strategic accounts and global partnerships. In his new role, Pencak will strengthen client relationships, scale commercial capabilities and deliver solutions to accelerate innovation across the life sciences industry. He is also active in the broader life sciences community, speaking at industry events on technology and artificial intelligence in clinical environments.