Offer summary

Qualifications:

Bachelor’s degree in a science or clinical related field., 9+ years of experience in the clinical research industry or a similar field., Strong problem-solving skills and ability to make decisions in ambiguous situations., Basic understanding of clinical study roles and financial tools related to project management..

Key responsabilities:

Lead and collaborate with global teams across multiple time zones.

Support project teams by coordinating activities and ensuring effective communication.

Interact professionally with internal and external colleagues to build rapport and trust.

Apply relevant guidelines and standards in data management and clinical trials.

Job description

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Skills:

• Ability to lead and collaborate with global teams. Motivate/guide virtual teams across multiple time zones and cultures to work effectively
• Negotiation skills and ability to influence, in order to achieve mutually beneficial results
• Good interpersonal, oral and written communication skills, using concise phrasing tailored for the audience with a diplomatic approach
• Learning ability and knowledge sharing approach; swift understanding of technologies and new processes
• A flexible attitude with respect to work assignments and new learning; ability to adjust rapidly to changing environments
• Basic presentation skills
• Customer focus to interact professionally and respectfully within Parexel and all external colleagues to build rapport and trust
• Commitment to first-time quality, including a methodical and accurate approach to work activities
• Time management and prioritization skills, in order to meet objectives and timelines
• Evidence of strong problem-solving skills, including capability to make appropriate decisions in ambiguous situations, ability to conduct root cause analyses.

Knowledge and Experience:

• 9+ yrs experience in clinical research industry or similar field
• Proven record of coordinating and supporting project teams
• Basic understanding or willingness to learn and apply Parexel financial tools, reports and processes for management of project financials with regards to forecasting, revenue recognition, scope of work and department budget for assigned projects
• Basic understanding of or willingness to learn Clinical Study Team roles outside of Data Management
• Full understanding or willingness to learn and apply relevant ICH-GCP Guidelines, local regulatory requirements and Parexel SOPs and study specific procedures
• Awareness of/or willingness to learn SDTM/CDISC/CDASH standards
• Awareness/potential prior experience in Clinical Trial/Data Management Systems (e.g. InForm, Rave, Veeva, DataLabs) and Microsoft Office products.
• Demonstrates technical aptitude.

Education:

Bachelor’s degree and /or other qualifications in a science or clinical related industry

Required profile