Thermo Fisher Scientific
Thermo Fisher Scientific
Thermo Fisher Scientific dezvoltă și furnizează tehnologii, produse de laborator și servicii farmaceutice care sprijină cercetarea științifică și asistența medicală. Activitatea sa acoperă cercetarea în domeniul științelor vieții, rezolvarea problemelor analitice, creșterea productivității laboratoarelor, diagnosticarea, precum și dezvoltarea și producția de terapii. Compania își deservește clienții printr-o echipă globală și un portofoliu de mărci care include Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon și PPD. Oportunitățile de carieră includ activitățile științifice, medicale, de producție, logistice și de servicii care susțin aceste oferte.

Remote Site Contract Specialist in Turkey

Manage investigator contracts, budgets, negotiations, and site activation activities for Thermo Fisher Scientific’s global clinical research services. This Turkey-based remote role covers compliance, risk management, contract operations, and support for country-level process improvement.

Descriere

  • Draft, review, negotiate, and finalize agreements with clinical study sites
  • Negotiate investigator grant budgets and contractual terms within approved parameters
  • Follow negotiation limits, approval requirements, contractual procedures, client expectations, budget guidance, templates, and operating procedures
  • Identify, evaluate, and appropriately escalate legal, financial, and operational risks
  • Recommend solutions and alternative approaches for Investigator Contracts negotiations
  • Coordinate with internal teams to align site startup and contracting work with timelines and site activation milestones
  • Meet established site activation cycle-time targets
  • Monitor activities and prepare required reports
  • Train and mentor junior team members
  • Contribute to country process improvements and team meetings
  • Serve as the country subject matter expert for Investigator Contracts training materials
  • Work with Global Site Contracts to maintain compliance with global processes and corporate directives
  • Conduct periodic quality reviews and complete peer feedback reports
  • Lead amendment and novation projects, and manage confidentiality agreement negotiations when required

Cerințe

  • Bachelor’s degree or an equivalent relevant academic or vocational qualification
  • At least five years of comparable experience demonstrating the knowledge, skills, and capabilities required for the role
  • Relevant education, training, or directly related experience may be accepted in combination
  • Detailed knowledge of contract law, including business, intellectual property, local tax, and stamp laws
  • Strong spoken and written communication skills in English and the local language
  • Ability to negotiate investigator grant budgets within approved parameters
  • High level of attention to detail
  • Excellent analytical and decision-making skills
  • Knowledge of pharmaceutical product development and the role of CROs
  • Ability to work effectively both independently and collaboratively
  • Strong organizational and time-management skills
  • Working knowledge of PPD SOPs and WPDs
  • Ability to manage competing priorities and assess contractual risks and issues
  • Proficiency with automated systems and computer applications
  • Customer-focused communication, problem-solving, and collaboration skills
  • Ability to independently train and mentor staff
  • Ability to provide constructive feedback to Investigator Analysts
  • Strong problem-solving and risk-assessment capabilities
  • Ability to negotiate Investigator Contracts in the best interests of the company and client

Beneficii

  • Fully remote working arrangement
  • Standard Monday-to-Friday schedule
  • Opportunities for training and mentoring
  • Collaboration and professional development within a global team
  • Meaningful work supporting life-changing therapies and better health outcomes

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