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Vice President, Biometrics

ErgomedRaleigh, North Carolina, United StatesRemote
This job is no longer open

Company Description


Ergomed PLC is a rapidly expanding full service mid-sized CRO specialising in Oncology and Rare Disease.  Since its foundation in 1997 the company has grown organically and steadily by making strategic investments and landmark acquisitions, with operations in Europe, North America and Asia Our company allows for employee visibility (you have a voice!) creative contribution and realistic career development.  We have nourished a true international culture here at Ergomed.  We value employee experience, well-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an environment from which a high-quality client service can be achieved. Come and join us in this exciting journey to make a positive impact in patient’s lives.  

Job Description


As the Vice President of Biometrics, you will serve as a key leader within our organization, responsible for overseeing the gloabl Biometrics department, which includes biostatistics, programming, data management, and medical writing teams. You will play a pivotal role in shaping our clinical trial data analysis and reporting strategies, ensuring the accuracy, quality, and integrity of all biometric-related activities.The VP, Biometrics is a senior member of the Leadership Team, reporting into the Executive VP.Responsibilities include:

  • Provide strategic leadership and mentorship to the biostatistics, data management, and medical writing teams
  • Develop and maintain a high-performing, collaborative, and results-oriented department
  • Develop core competencies of the group, foster a culture of continuous improvement and innovation within the team.
  • Develop infrastructure/processes and best practices for the function
  • Ensures high quality of all services and deliverables provided by Biometrics.
  • Monitors progress of projects against budget for Biometrics.
  • Develop benchmarks for tasks re time, budget, quality
  • Responsible for functional resource allocation; assign functional resources for each project based on scope of services in the proposal/contract; supervise to ensure timely and quality delivery of the service and provide guidance and support to the functional representative on each project as needed.
  • Responsible for budget, forecast and profitability of the functional services for each project
  • Provides strategic consulting to clients on their product development strategy, including development options, statistical study design, specification of endpoints, and sample size determination/justification.
  • Actively participates in Business Development (BD) process as a subject matter expert by providing strategic and tactical input at bid defenses.
  • Participates in the generation of proposals.
  • Represents the Company by attending industry meetings, speaking engagements, participating in booth exhibitions, etc., and by publishing scientific or industry related articles in industry journals.

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Qualifications


  • Degree qualified in a Biometrics/Life Science related subject
  • Demonstrated experience working in a CRO environment leading a global biometrics team including statistics, programming, data management and medical writing
  • Record of driving and executing biometrics strategy
  • In depth knowledge of the drug development process, worldwide regulatory requirements, clinical trial methodology and complex statistical designs
  • Excellent leadership and management skills
  • Demonstrated ability to lead cross-functional teams
  • Ability to handle multiple tasks to meet deadlines in a dynamic environment
  • Effective organizational, presentation, documentation and interpersonal skills
  • Effective problem solving and decision making
  • Exceptional communication skills and the ability to collaborate effectively with internal and external stakeholders
  • Strong customer focus

Additional Information


We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow.  To succeed we must work together with a human first approach. Why? because our people are our greatest strength leading to our continued success on improving the lives of those around us. 

This job is no longer open

Life at Ergomed

Founded in 1997, Ergomed is a global provider of high-quality services to the biopharmaceutical industry, spanning all phases of clinical trials, post-approval pharmacovigilance, and medical information. Ergomed’s fast-growing services business includes an industry-leading suite of specialist pharmacovigilance (PV) solutions, integrated under the PrimeVigilance brand, and Ergomed Clinical Research, a complete, global Phase I-IV clinical development and trial management services with a strong heritage in the development of drugs in rare diseases and oncology. • 1,400+ highly qualified professionals • Global full-service CRO • 25+ years of experience • Therapeutic specialization in oncology • Strong expertise in rare disease trials • Robust clinical safety system • Choice of leading drug safety databases Our key services include: • Clinical Research Services • Pharmacovigilance • Medical Information • Regulatory • Medical Writing • Site Management • Study Physician Support • Biostatistics • Patient Study Support
Thrive Here & What We Value1. Emphasis on personal and professional growth2. Friendly, supportive working environment3. Opportunity to work with colleagues globally (English as company language)4. Diversity, equity, inclusion, equal opportunities5. Human-first approach for success6. Employee visibility and creative contribution7. Realistic career development8. Healthy work-life balance
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