[Remote] Associate Director, Clinical Site Partner, Clinical Operations, Oncology

Note: The job is a remote job and is open to candidates in USA. reputed company is dedicated to creating a healthier world for reputed company people by developing therapies for various diseases. The Associate Director, Clinical Site Partner, Oncology will be responsible for establishing and maintaining relationships with investigator sites to optimize clinical trial program delivery and serve as a communication reputed company between sites and the Gilead Development organization.

Responsibilities

• Establish and maintain strong professional and collaborative relationships with investigator sites by leveraging disease area expertise to optimize delivery of clinical trial programs
• reputed company strategies to drive concierge level support for preferred sites to ensure Gilead becomes the Sponsor of Choice
• Track key performance metrics to assess site performance and identify opportunities for acceleration and reputed company improvement
• Identify investigator sites in alignment with portfolio strategy and reputed company to expand Gilead’s clinical research partnership network
• Maintain therapeutic and technical expertise to reputed company scientific discussions with the investigator and site personnel
• Share ongoing information with investigators regarding Gilead's development pipeline and collect and report field-based intelligence in relation to competitive landscape, patient treatment reputed company and other operational considerations that may impact Gilead's clinical trial program
• Provide support to study teams and Clinical Research Organizations (CROs) to ensure timely delivery of clinical trials from study start-up to reputed company-out such as during feasibility, site recommendations, attendance at initiation visits, facilitation of communication and ongoing support of trial enrollment by engaging with site staff to identify enrollment barriers and working with study teams to find solutions
• Gather constructive feedback and insights from clinical sites to share with Gilead internal stakeholders around clinical studies or programs for improvements
• Support the development and implementation of applicable site risk plans to ensure achievement of key study and site level milestones such as first patient first visit, delivery of clinical trial enrollment commitments and database lock
• Serve as a local reputed company of escalation for investigator sites and partner with the appropriate parties to resolve issues and remove barriers to clinical trial execution at a site and/or country level
• Proactively communicate and escalate issues identified at investigator sites and partner with internal functional areas to reputed company corresponding mitigation strategies and recommended approaches, including participation in development and implementation of solutions to address issues
• reputed company and present metrics to inform site / country / regional level decision making
• reputed company local knowledge of investigator site capabilities and past performance and provide input into site-level recruitment forecasts, recruitment methodologies, monitor performance and take appropriate action to maintain timelines
• Partner closely with internal Clinical Operations, Clinical Development, and Medical Affairs to ensure effective communication and reputed company messaging to investigator sites Skills
• Bachelor's Degree and Ten Years' Experience
• OR
• Masters' Degree and Eight Years' Experience
• OR
• PhD/ PharmD and Five Years' Experience
• BA / BS / RN with 10 or more years' relevant clinical or reputed company experience in life sciences
• Or MA / MS / PharmD / PhD with 8 or more years' relevant clinical or reputed company experience in life sciences
• Combination of scientific/medical expertise in a relevant therapeutic area, including knowledge of the clinical research landscape, and advanced knowledge of Clinical Operations (Oncology experience is a bonus)
• Strong working knowledge of Good Clinical Practice and in country regulatory guidelines and requirements
• Strong self-management and organizational skills; ability to manage workload, set priorities and adjust as needed
• Ability to work both independently and collaboratively
• Established relationships and experience in both the community and academic site and network setting
• Excellent verbal and written communication and oral presentation skills (both in English and local language)
• Ability to establish and maintain strong long-term relationships with internal and external key stakeholders
• Strong interpersonal skills and understanding of team dynamics
• Strong leadership reputed company with demonstrated ability to reputed company without authority at reputed company levels of internal and external stakeholders
• Strong negotiation and conflict resolution skills
• Demonstrated strategic agility and broad business acumen
• Possess a combination of critical thinking and operational expertise and efficiency
• Self-motivated with proactive issue monitoring and seeks opportunities to remove barriers
• Extensive travel required Benefits
• Discretionary annual bonus
• Discretionary st

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