· Manage and oversee departmental activities including appropriate resourcing of staff, staff assignments, and quality control/timely delivery of project deliverables· Participate in and contribute to project bids, including client presentations· Drive team members to improve their efficiency and effectiveness at prioritizing work and improving performance evidenced by the work produced, client feedback, audit results, and QC measures· Implement process improvements, in conjunction with Management team and Quality Management Group, in response to client and team feedback and quality audits· Revise, implement, and monitor departmental compliance with SOPs· Work with senior departmental management in developing managers and ensuring a talented pipeline of management staff within the department or function· Undertake the full range of duties relevant to the leadership, management, and development of the team to ensure their performance meets and or exceeds both the business and their own personal goals/objectives· Participate in formal staff review processes· Support efforts for generating business leads

Over the past 30 years, PAREXEL has developed significant expertise to assist clients in the worldwide pharmaceutical, biotechnology and medical device industries with the development and launch of their products in order to bring safe and effective treatments to the global marketplace for the patients who need them. Headquartered near Boston, Massachusetts, PAREXEL operates over 78 locations throughout more than 52 countries around the world, and has over 14,400 employees.We are a leading global bio/pharmaceutical services organization that helps clients expedite time-to-market through our development and launch services. These include a broad range of clinical development capabilities, integrated advanced technologies, regulatory affairs consulting, and commercialization services.

Our late phase research team is uniquely positioned to deliver intelligence that allows you to address key areas throughout commercialization that include: Post-authorization safety studies (PASS) / Post-authorization efficacy studies (PAES) Phase IV trials—approved product, same indications (interventional) Registries—disease, product, and safety (observational) Consumer healthcare/OTC trials Community-based and naturalistic studies Health economic piggyback trials Scientific disseminationOutput from late phase initiatives underpins all of these solutions while a dedicated team of full-time employees supports your commercialization areas of concern with proven expertise. The level of integration and interconnectivity we deliver—providing you with all of your essential commercialization solutions under one roof—leads to greater efficiency and quality.

ICON is a global clinical research organization that provides outsourced development services to the pharmaceutical, biotechnology and medical device industries. It specializes in the strategic development management and analysis of programs that support clinical development from compound selection to Phase I-IV clinical studies.

ICON is a global clinical research organization that provides outsourced development services to the pharmaceutical, biotechnology and medical device industries. It specializes in the strategic development management and analysis of programs that support clinical development from compound selection to Phase I-IV clinical studies.

Cognitive Drug Research Ltd. offers a complete solution to cognitive assessment in clinical trials. We provide expert advice on protocol design as well as appropriate loading, measurements and testing schedules. CDR supplies all the necessary testing equipment and investigator training to administer multiple sites around the globe. We receive, manage, analyse, interpret and report the resulting data in formats acceptable to international regulatory bodies.For cognitive assessment in pharmaceutical development worldwide, the simple solution is CDR.

Cognitive Drug Research Ltd. offers a complete solution to cognitive assessment in clinical trials. We provide expert advice on protocol design as well as appropriate loading, measurements and testing schedules. CDR supplies all the necessary testing equipment and investigator training to administer multiple sites around the globe. We receive, manage, analyse, interpret and report the resulting data in formats acceptable to international regulatory bodies.For cognitive assessment in pharmaceutical development worldwide, the simple solution is CDR.

I spent several months in The Gambia, West Africa working with Gambians on community health and education. This involved teaching math as well as everyday health methods to improve the general quality of life. I lived in several small towns and was fully immersed in the culture.