Lead Data Manager

About us

Based in Parma, Italy, Chiesi is an international research-focused pharmaceuticals and healthcare group with over 85 years’ experience, operating in 30 countries with more than 6,000 employees (Chiesi Group). To achieve its mission of improving people’s quality of life by acting responsibly towards society and the environment, the Group research, develops and markets innovative drugs in its three therapeutic areas: AIR (products and services that promote respiration, from new-born to adult populations), RARE (treatment for patients with rare and ultra-rare diseases) and CARE (products and services that support special care and consumer-facing self-care).
We are proud to be the largest global pharmaceutical group to be awarded B Corp Certification, a recognition of high social and environmental standards. We are a reliable company that adopts and promotes transparent ethical behavior at all levels. 
We are committed to embrace diversity, inclusion and equal opportunities. In fact, we are a global family made up of different cultures, different genders, generations, ethnicities, abilities, sexual identities and many other enriching diversities. 

Chiesi USA

Chiesi USA is a specialty pharmaceutical company focused on developing and promoting products for the hospital, adjacent specialty and rare disease markets. We are a B Corp™ and Benefit company awarded Top Employer status for six consecutive years and certified as a Great Place to Work. 
At Chiesi, we share an entrepreneurial spirit and act as a force for good, pursuing high social and environmental standards, to ensure the wellbeing of our people, patients, and communities. We offer a work environment where professionals have the opportunity to build a purposeful career focused on helping others while achieving a fulfilling work-life balance, meeting exciting challenges, and engaging in important and rewarding work.

What we offer

Chiesi offers competitive benefits, services, and programs that enrich the personal and professional lives of our employees.   Our shared values of passion, innovation, trust and integrity bring out the individual talents and diverse perspectives of each of our colleagues.  Our environment encourages each individual to reach his or her full potential and drive outstanding results. We celebrate that “Every one of us is different. Every one of us is Chiesi."

Purpose

• To lead data management activities of the assigned project(s) ensuring data strategy and data governance are properly implemented across all clinical studies 
• To act as technical leader supporting team members, ensuring consistent data management approach across studies, and representing data management at project level
• To ensure technologies/systems/data platform needed for collecting and handling clinical data are properly developed, tested, fit for purpose and integrated
• To ensure data management activity of the assigned projects are planned and executed according to project timelines, with highest standards in data integrity and data quality and under budget control
• To define the strategy for data submission and lead the preparation of the data package to be submitted for drug approval 
• To represent Data Management in case of audit and Regulatory Inspection

Main Responsibilities

• To plans and drive the conduct of all Data Management activities for the assigned project(s) ensuring consistent approach across studies
• To manage high complex studies and/or support specific activities of studies managed by other data managers or consultants
• To provide technical tutoring and supervise data managers and/or contractors assigned to clinical studies of the project by conducting regular reviews of activity status 
• To manage and guide providers, setting requirements, preparing or reviewing Request for Proposals and monitoring performance 
• To regular monitor data management costs of the assigned studies ensuring respect of budget
• To define and proactively manage risks with potential impact on study systems setup, study conduction, or reliability of study results
• To ensure all data collection systems for assigned projects are setup, tested and fit for purpose according to expectations and timelines
• To lead the data quality evaluation, by the investigation of all clinical and operational data, evaluating trends, deviations, using visual analytics tools and ad hoc reports
• To define the strategy and lead the preparation of data package for regulatory submission
• To represent data management for auditing / regulatory inspection 

Addi