Head of Life Sciences Consulting
4 weeks ago
We are a fast-growing industry leader in the TMF (Trial Master File) Services, Inspection Readiness and Clinical Compliance (GCP) Consulting space. Our team of professionals assist biotech and pharma companies develop and streamline compliant processes, proactively prepare for regulatory inspections, implement and optimize eClinical technologies, and provide an efficient and effective resourcing strategy for Sponsor oversight and TMF management.
Job SummaryWe are seeking a highly experienced professional to lead our consulting services for life sciences companies. The ideal candidate will have a strong understanding of market dynamics and customer needs in eClinical professional services offerings, as well as experience leading teams of consultants and managing the business aspects of a consulting group.
Responsibilities- Develop and implement strategy for positioning The O'Connor Group as a best-in-class consulting service provider to Pharmaceutical and Biotechnology companies
- Develop an overall strategy for delivery of consulting services and for growing the consulting business
- Provide Thought Leadership for the organization and create strategies that strengthen the company's role and position related to eClinical Consulting
- Significant contributor during consulting-related Business Development
- Lead and manage a team of consultants
- Manage the business aspects of the Consulting group based on goals and targets set by senior leadership
- Act as Subject Matter Expert (SME) and/or Consulting Lead
- Minimum of 10-15 years of experience in Pharmaceutical and/or Biotechnology professional services
- Minimum of 10-15 years of experience in the within a life sciences consulting organization
- Minimum of 2 years small company professional services experience, extensive experience leading consulting projects
- Experience leading teams of consultants
- Strong understanding of market dynamics and customer needs in eClinical professional services offerings
- Working knowledge of international regulatory record requirements and ethics requirements that relate to the Clinical domain
- Experience leading consulting groups/practices and large work teams
- Strong knowledge of drug development process
- Strong leadership skills
- Excellent communication skills
- Excellent problem-solving skills
- Bachelor's Degree Required
- Travel – up to 30%
- Position is a remote/virtual position.
- Compensation package that recognizes your expertise and contributions.
- Flexibility in your schedule, promoting work-life balance. This includes Paid Time Off, paid holidays, winter break, and "half day Fridays" during the summer.
- Comprehensive range of healthcare options for you and your loved ones, including medical, dental, and vision plans (premium cost is shared between you and us), along with life insurance and short-term income replacement plans.
- Assist in your future financial well-being with a 401(k)-savings plan including a company match.
- A vibrant, enthusiastic team of individuals who are passionate about what they do and who they work with.
To be eligible for consideration, candidates must be located in Pennsylvania, North Carolina, Kansas, Missouri, Florida, Indiana, Virginia, South Carolina, Texas, New Jersey, Georgia, Massachusetts, or New Hampshire.
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