Associate Director, Clinical Development job opportunity at Gilead Sciences.

Home Jobs In Japan Tag: Clinical Development Associate Director, Clinical Development position at Gilead Sciences


bot
Gilead Sciences Associate Director, Clinical Development
Experience: Highly Experienced
Pattern: full-time
Country:
apply Apply Now
Salary:
Status:

Clinical Development

Copy Link Report
degreeAssociate
loacation Japan - Tokyo, Japan
loacation Japan - Tokyo....Japan

At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.   Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.   We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together. Job Description   Specific Job Requirements Reporting to the therapeutic head in Clinical Development Japan, this position in Clinical Development plays an integral role in the scientific planning, execution and reporting of Japanese clinical studies for Gilead’s development compounds in inflammation and virology therapeutic area. Although generally assigned to a specific therapeutic area, this position may support local clinical development activities across development programs including oncology. The overall responsibilities of this position include the following: 1 Acts as the local scientific expert for assigned clinical research activities, addressing questions from internal functions and external Japanese physicians and research scientists. - Works with Gilead Sciences Inc., (GSI) project teams including biostatisticians to prepare analyses to address specific questions as required. 2 Drive assigned projects forward as Japan project team (JDT) lead with Japan cross functional team members. Interact regularly with Global Development Team (GDT) Lead to exchange project information including strategic aspects. Provide local requirements and needs to GDT Lead. 3 Provides scientific support to Gilead functions including but not limited to GSI Clinical Development, Clinical Operations, Biostatistics, Data Management, Medical Writing, Clinical Pharmacology and Medical Affairs. Provides guidance to ensure scientific and clinical issues are addressed in a consistent manner. 4 Responsible for identifying, establishing and maintaining science-based relationships with Japanese therapeutic area experts to support Gilead’s development programs. 5 Responsible for the design of Japanese clinical studies including authoring of study concepts and protocol synopses. Works with the Clinical Operations team for the development, finalization and amendment (as applicable) of study protocols. - Ensures scientific and clinical consistency across Japanese study protocols and with the global development programs. - Retains overall responsibility for the scientific content and scientific integrity of clinical trials conducted in Japan. - Proposes membership for ‘Trial Guidance and Publication Committees (TGPC)’ for review by GSI Clinical Development. - Prepares specific sections of clinical study manuals, Investigator Meeting notebooks and other documents are needed. - Contributes to the design and development of CRFs, Data Management Manuals and Data Analysis plans. Acts as the Study Director or Medical Monitor for assigned clinical studies in Japan. 6 Prepares and presents （if applicable） scientific information concerning Gilead’s development programs internally and at external meetings as required. - Prepares abstracts, posters and oral presentations of Gilead’s clinical trial and associated data for Japanese scientific meetings. - Provides input for manuscripts containing Japanese data prior to Journal submission. - Coordinates the preparation and/or review of data listings, summary tables, study results, scientific presentations & manuscripts for publication - Critically assesses abstracts, posters, oral presentations and manuscripts received from Japanese therapeutic area experts proposed for submission to local Japanese scientific meetings or Journals. Collaborates with the requestor concerning content. - Ensures review and approval of all of the above by the respective GSI Project Team prior to submission, presentation and/or publication. 7 Critically assesses requests from Japanese therapeutic area experts for clinical development studies, Investigator Sponsored Trials (ISTs) and Grant requests: - Ensures alignment of such requests with Gilead’s scientific strategies and global activities - Ensures all requests are evaluated in accordance with GSI procedures and is responsible for subsequent negotiation of changes and/or communication of Gilead position with Gilead Medical Affairs (if applicable) and the requestor. 8 Responsible for drafting regulatory Briefing Documents and slide presentations for use at PMDA and MHLW meetings. Attends and presents Gilead position at informal and official Consultation meetings with PMDA and MHLW. 9 Working with Regulatory Affairs and the respective GSI Project Team, prepares written responses to PMDA, MHLW and IRB queries. 10 Coordinates the preparation and/or review of regulatory documentation including but not limited to IND annual reports, IND safety reports, Investigator Brochures and J-NDAs. - Conducts all responsibilities in accordance with Japanese regulatory requirements, industry standards, GCP and Gilead Standard Operating Procedures (SOPs). Candidates must have the following essential experience: Experience with regulatory-related document drafting and query responses Experience drafting the clinical module of the CTD (not just reviewing), and preparing responses to PMDA queries, which lead to approval Experience drafting briefing documents or protocols for PMDA consultations and preparing responses to PMDA queries Strong experience discussing development plans with cross-functional teams such as Regulatory, Operation, Commercial, Market access Experience presenting Japan development plans with other functions in Japan and with global teams in the US/EU Excellent English and Japanese communication skills Specific Education and Experience Requirements ・MS degree or above. ・Minimum of 10 years of project leading experience within clinical research / clinical development. ・Experiences in preparing the CTD and query responses in JNDA. ・Leadership and project management skill to drive clinical development of new therapies in Japan. ・Communication skill enabling timely information sharing with GSI and other functions at Gilead Japan. Smooth language skill for English and Japanese, English level is expected at TOEIC> 900 or TOEFL iBT>90. ・Problem solving skill to analyze the problem and develop/execute action plans. ・Medical writing skill to prepare study protocols and regulatory documents related to clinical. ・Negotiation skill with investigators and officials in the Health Authorities to move the study forward. ・Deep knowledge of clinical guidelines and regulatory requirements. ・Extensive experiences in clinical development to put together the best and fastest development strategy. ・Up-to-date expertise in the responsible therapeutic area.   For Current Gilead Employees and Contractors: Please apply via the Internal Career Opportunities portal in Workday.

Other Ai Matches

Director, Lab Operations Applicants are expected to have a solid experience in handling Lab Operations related tasks
Head of Manufacturing Strategy and Operations Applicants are expected to have a solid experience in handling Job related tasks
Sr Director - U.S. Ethics & Compliance Advisor Applicants are expected to have a solid experience in handling Job related tasks
Order to Cash Specialist Applicants are expected to have a solid experience in handling Job related tasks
Intern - IT - Enterprise Data and Analytics Applicants are expected to have a solid experience in handling Job related tasks
Therapeutic Specialist HIV-Franchise (m/f/d) Region Bayern and parts of Baden Württemberg Applicants are expected to have a solid experience in handling Job related tasks
Senior Director, Market Research, HIV Prevention Integrated Insights Applicants are expected to have a solid experience in handling Market Research, HIV Prevention Integrated Insights related tasks
Sr Director, Global Policies and Training Applicants are expected to have a solid experience in handling Global Policies and Training related tasks
Sr Associate Scientist- Inflammation Biology Applicants are expected to have a solid experience in handling Job related tasks
Associate Director, Regulatory Affairs CMC Applicants are expected to have a solid experience in handling Regulatory Affairs CMC related tasks
remote-jobserver Remote
Sr Manager, Commercial L+D - Nurse Educator & PrEP Lead Applicants are expected to have a solid experience in handling Commercial L+D - Nurse Educator & PrEP Lead related tasks
Director, External Quality Strategy and Operations Applicants are expected to have a solid experience in handling External Quality Strategy and Operations related tasks
Senior Director, Epidemiology Applicants are expected to have a solid experience in handling Epidemiology related tasks
Sr Mechanical Engineer II Applicants are expected to have a solid experience in handling Job related tasks
Scientist, Translational Inflammation Applicants are expected to have a solid experience in handling Translational Inflammation related tasks
Intern - Global Medical Affairs - HIV Team Applicants are expected to have a solid experience in handling Job related tasks
Scientist — Quality Control Biologics (Analytical Lifecycle Management) Applicants are expected to have a solid experience in handling Job related tasks
Sr QA Specialist Applicants are expected to have a solid experience in handling Job related tasks
Director, Clinical Development (MD) Applicants are expected to have a solid experience in handling Clinical Development (MD) related tasks
Sr Manager, Medical Affairs (Liver) - Hybrid MSL Applicants are expected to have a solid experience in handling Medical Affairs (Liver) - Hybrid MSL related tasks
Director, Marketing Sciences HIV PrEP Applicants are expected to have a solid experience in handling Marketing Sciences HIV PrEP related tasks
Senior Director, Product Management Team Lead (Late Phase & Commercialization) – Foster City Applicants are expected to have a solid experience in handling Product Management Team Lead (Late Phase & Commercialization) – Foster City related tasks
Cell Therapy Account Manager (CTAM) Region: Dresden / Leipzig / Magdeburg Applicants are expected to have a solid experience in handling Job related tasks