Andreea Dobrita

Senior Manager Gro, Leads at Parexel

Based in Romania

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Seniority

Manager

Department

Other

Location

Romania

Industry

Pharmaceutical Manufacturing

Company size

20K

Contact information

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Email

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a•••••••@parexel.com

Phone

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Background

About Andreea Dobrita

Clinical Operations Senior Manager with broad background in pharmaceutical industry over 24 years. Extensive experience for more than 15 years in clinical research within PAREXEL with a progressive carrier starting from CRA, continuing in the Clinical Lead / Clinical study Manager role. Managed large international studies in various therapeutic areas (Epilepsy, Multiple sclerosis, Heart Failure, Rheumatoid Arthritis, Multiple Myeloma, macular degeneration, osteoporosis ) conducted in Europe, North America and South America. From 2008 over 3 years managed a team of up to 25 CRA and CRA assistants and since 2011 more than 15 Clinical Operation Leaders located in Romania, Czech Republic, Serbia, Poland, Ukraine, Spain and South Africa Attended successfully Bid Defense Meetings and other Client meetings. Areas of strength are team leadership, problem solving attitude, strategic and business oriented thinking, excellent communication skills, efficiency and forward planning. Good motivator for the team driving them to achieve planned goals and timelines. As a manager also supported the COL team with any project issues raised on their studies, coaching and mentoring on the project level based on the phase of the project. Involved in project escalations also looking for solution to the most complex project issues. When needed acted as back-up for COL team at the project level covering all the COL tasks as required. Worked also as COL on several projects in the last years, being responsible for the oversight and coordination of the clinical team and being the liaison between project leadership and clinical team and ensuring the clinical deliverables. Managing regional hiring and resourcing process for Europe for Biotech Division. Strong professional skilled in Good Clinical Practice (GCP), Clinical Research, CRO Management, Clinical Monitoring, and Clinical Trial Management System (CTMS).

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