Jobs in Japan
Explore hand-picked jobs in Japan for English speakers across tech, education, marketing, and more.
Vetted companies only. Apply from overseas.
Explore hand-picked jobs in Japan for English speakers across tech, education, marketing, and more.
Vetted companies only. Apply from overseas.
Johnson & JohnsonAt Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com. As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Responsible for the development and analysis of site contracts including but not limited to drafting, negotiating, and finalizing agreements related to clinical trials and/or overseeing a Clinical Research Organization responsible for contract negotiations. The lead will assist with training of staff, facilitating clear and concise communications and assist Analysts with resolution of contracting and study related issues. In addition, the lead will provide project management and oversight to internal and external stakeholders as required and support to the clinical team in the pricing, planning, execution and control of contracts. Exemplary customer focus with vision to drive solutions. This is not an exhaustive, comprehensive listing of job functions. Other duties may be performed as assigned.
- Bachelor’s degree in appropriate scientific or business disciplines - 3 to 5 years-experience and/or equivalent competencies in pharmaceutical industry/clinical research - Must have a working knowledge of the clinical development process with 2 years of negotiation and contract experience - Excellent communication skills (both oral and written) - Familiarity with healthcare compliance and other relevant guidance (HIPAA, FCPA, Safe Harbor, etc.) Comprehensive knowledge of clinical research processes - Ability to work effectively in cross functional teams - Strong initiative and proven self-starter - Strong and proven negotiation and problem resolution skills - Working knowledge of PCs (MS Office suite at a minimum) and database management - Must demonstrate innovative spirit, have strong interpersonal skills, and ability to accomplish substantial tasks with minimal supervision; previous experience working in virtual teams preferred
- Analytical Reasoning - Clinical Research and Regulations - Clinical Trial Designs - Clinical Trial Management Systems (CTMS) - Clinical Trials - Communication - Data Savvy - Laboratory Operations - Organizing - Problem Solving - Productivity Planning - Professional Ethics - Project Integration Management - Quality Assurance (QA) - Regulatory Compliance - Research and Development - Research Ethics - Standard Operating Procedure (SOP)
