Role 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.
Key Responsibilities:
-
Provide high quality, timely, scientific/strategic solutions to meet client needs.
-
Understand client objectives and project specific requirements to customize delivery to the client need; apply innovative evidence strategies.
-
Lead the conduct and analysis research, that will shape the development of strategic recommendations, under the guidance of the project director.
-
Manage and contribute to the execution of tasks to search for evidence as part of the literature review (e.g. screening, data extraction, protocol design, quantitative feasibility) to support the overall client objective.
-
Manage and prepare the synthesis and review of findings.
-
Develop project deliverables as required in a typical Systematic Literature Review project e.g. systematic review reports, slide decks, manuscripts, abstracts and posters.
-
Produce and ensure quality work that meets the expectations of Project Lead/ Manager and the client.
-
Work within broad project guidelines as directed by the Project Director and/or Technical SMEs.
-
Take initiative to prioritize work to achieve specified project outcomes while confirming alignment with Project Lead and Line Manager.
-
Follow and implement the organization’s consulting models and methodologies.
-
Lead on all aspects of project management activities.
Parexel – Related Responsibilities
-
Complete basic job-related responsibilities, including timesheets, expense reports, maintenance of CVs, project deliverable archiving.
-
Participate in internal initiatives/projects or as a mentor as requested by management.
Qualifications
-
Strong computing skills (MS Office)
-
High analytical ability
-
A high degree of written accuracy and attention to detail
-
Good communication skills, both oral and in writing, especially in the relaying of technical information
-
Self-motivation, enthusiasm
-
A flexible attitude with respect to work assignments and new learning
-
Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail
-
Fluent English, with excellent verbal and written skills essential
-
Keen interest in medical research, provision of healthcare and the pharmaceutical industry
Requirements
-
Training and/or experience in health economics and/or outcomes would be an advantage.
-
Minimum 4 years experience in a relevant role would be advantageous.
Education
-
Master’s degree or equivalent in Life Science/MBBS/BDS/PhD is essential.