Who are we?
As a top five CRO, providing innovative solutions for our clients is what we do. From full service clinical development to the pioneering Embedded SolutionsTM model, PRA provides a broad spectrum of solutions that meet the demands of a diverse marketplace.
At PRA, borders do not create boundaries. Our growing workforce is 15,000+ employees strong, spanning 13 time zones across 85 countries – yet we operate in unison as one global community. We are committed to saving lives and we are constantly striving to be the best at what we do. Our impact is real and we see it every single day. We help get life-saving drugs into the hands of those who need them most.
Who are you?
You are a forward thinker. You are an innovator that refuses to settle. The idea of using your technical skills to support a global community that works diligently towards improving the lives of others excites you. You want to push the boundaries and change the future. You want to learn from the best, grow your knowledge and your skill set, and you want to build your career. You want to use the latest technology and tools in the industry to push the momentum of an already growing company forward. You want to find a balance that still lets you be, well, you. Most of all, you want to do it in a place where you’re more than an employee number…a place you love working.
Still here? Good. If this is you, we’d really like to meet you.
We are looking for a Trial Manager (TM) based in India.
As a Trial Manager, you will be dedicated to one of our global pharmaceutical clients, a company that values performance, recognizes merit and has a high focus on quality. This environment encourages innovation, individuality and embraces people that want to be a part of it.
We are seeking an experienced Trial Manager to work as an integral part of our pharma client’s global study team. The key function of the Local Trial Manager is to provide operational country oversight and monitor progress of local activities of global studies by project managing a clinical team at a country level.
Working throughout the lifecycle of the trial, from start-up through to database lock and closure activities, key responsibilities will include:
A typical working day may include creating study documents, meeting with your team, sharing your expert local knowledge with other internal collaborates and even involvement with process improvement initiatives at a more global level. You will truly be a local study expert and will be expected to leverage your experience.
Organised, creative and confident in taking independent action.
To ensure success within this role, the following are required:
Your health, your family, your career, your money — the things that matter to you, matter to us. The benefits of PRA just get better and better.
PRA Health Sciences is an Equal Opportunity Employer. We welcome and encourage diversity in the workplace.