Job details
Job type full-time
Full job description
Job overview:
Iqvia™ real-world evidence (rwe) teams work with clients to help them collect and use real-world data to generate evidence to meet the needs of regulators, payers, providers and patientsOur approach is unique in the industry and is defining the way companies can develop and apply real-world evidence to provide deeper insight about market dynamics, therapy area changes, outcomes research and other scientific insightsWe are collaborative, intellectually curious, entrepreneurial and constantly looking for opportunities to harness the value of real-world evidence in a constantly evolving industry.
Rwe project management is at the cornerstone of our study delivery and responsible for ensuring high-quality delivery to help our customers generate critical evidenceRwe project management is creating and delivering the next generation of late phase studies, emphasizing creative problem solving and looking for individuals interested in changing the way research is conducted.
The associate director position is a critical role in our team, using expertise to guide study teams and be accountable for creating strong client relationshipsThe role also is involved in helping the senior leadership identify and solve for industry trends while also managing the work force required to deliver to an excellent standardWe ask our associate directors to wear multiple hats and give them the opportunity to also lead high visibility strategic initiatives along side day to day study delivery.
Iqvia is looking for energetic professionals with in-depth project management experience who have an appetite for career growth, innovation and leadership.
Qualifications:
Bachelor`s degree life sciences or related field required
Requires advanced knowledge of job area, and broad knowledge of a other related job areas, typically obtained through advanced education combined with experience.
Requires in-depth clinical research experience including project management experience or equivalent combination of education, training and experience.
Knowledge of clinical trials - knowledge of clinical trial conduct and skill in applying applicable clinical research regulatory requirements i.eIch gcp and relevant local laws, regulations and guidelines, towards clinical trial conductBroad protocol knowledge, therapeutic knowledge desiredGood understanding of the competitive environment and how to communicate/demonstrate value through iqvia solutions.;
At iqvia, 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 worldThe advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the wayLearn more at jobs.iqvia.com.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.
Iqvia, incProvides reasonable accommodations for applicants with disabilitiesApplicants who require reasonable accommodation to submit an application for employment or otherwise participate in the application process should contact iqvia’s talent acquisition team at workday_recruiting@iqvia.com to arrange for such an accommodation.
