Job Responsibilities:

• Work closely with development team to provide solid support to trial implementation in terms of site/investigator recommendation, trial start-up, initiation, patient recruitment, etc.

• Review and accountable for brand medical plan and launch readiness medical plan.

• Ensure and responsible for compliance and quality in external material review and medical affairs studies implementation.

• Provide timely medical support to DRA team in terms of NDA approval, PAC implementation, license renew, license updates, safety updates, etc.

• Leading scientific communication strategies and Medical Activities

• Lead cross functional team to manage crisis and risks with drug safety and quality control.

• Supervise the implementation of Medical Affairs Studies

• Lead the full scope of Medical affairs studies (Phase IV/PMS, IIT and epidemiological researches) and publication plan to be aligned with the brand strategy.

• Chair TA related protocol review meeting, participate brand meeting and Global medical team meeting to ensure strategy alignment globally and locally.

• Work with Clinical operation team to facilitate global trials in the region.

• Drive scientific engagement with their Medical Experts. Implement clinical and educational strategies and respond to unsolicited medical enquiries.

• Engage with Medical Experts (MEs) to educate on medical/scientific information

• Prepare and execute TA medical strategy and tactic plan to work with Development, Marketing, to synergize and prioritize medical affairs trials and activities in align with business strategy and objectives.

Qualifications:

• The individual shall possess both field medical and clinical experience in oncology (solid tumors) and rare diseases and ideally have relationship with the clinical sites in the country

Additionally the MSLs shall possess the following skills:

• Strong presentation, communication and negotiation skills

• Understand the relationship between field medical, clinical operations and commercial counterparts

• Ability to create and sustain relationships with investigators and other professional at the clinical sites

• Have an in-depth understanding of the clinical trial process and of pharmaceutical product development and approval.

• Ability to clearly articulate complex scientific and clinical data in 1:1 and group settings

• Demonstrated success in prior roles and ability to manage large territories/ multiple geographies as needed

• Ability to work independently and cross functionally within teams

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com