At Clintec, we know where people’s lives are involved there is way more to be done. That is why every person assigned to our projects is working hard to find innovative ways towards improving the health and lives of millions. Clintec delivers global clinical projects with speed, efficiency and cost-effectiveness, but don’t just take our word for it - as winners of numerous awards for service delivery, business leadership and entrepreneurship over the years, we know what good looks like!
We are looking for an experienced Clinical Project Manager (PM) in the UK who has experience working at a global level to join our team on a full-time and permanent basis.
Working for Clintec:
At Clintec, our staff never stop learning. Join them and receive expert training and guidance throughout your career, get the opportunity to move up the career ladder and travel globally (up to 40%). We believe our people are our greatest asset and understand that the best performance comes from individuals who know they are valued and supported by their teams.
We look after our staff and work/life balance is important to us. We are proud of our people and family friendly policies.
We can offer you:
A competitive salary, car allowance, 25 days annual leave, an extra day annual leave on your birthday, flexible working hours, private healthcare, pension contribution, life assurance and a friendly and social working environment
The opportunity to work with various global pharmaceutical leaders on the some of the most prestigious, ground-breaking and challenging drug development projects
Real career development opportunities and a life-long career with an innovative, forward-thinking clinical research company
As a Clinical Project Manager (PM) you will thrive in a fast-paced environment where you will be responsible for leading one or more clinical trials simultaneously and be responsible for end-to-end project management activities including initiation, conduct, tracking and reporting of clinical trials. You will be responsible for coordination of the project team ensuring the study is delivered within budget, within the timelines and on target according to the requirements of the study specific contract.
Does this role meet my skills/experience?
The ideal candidate should have a bachelor’s degree (higher or equivalent) in a life science discipline with a significant track record within clinical project management, preferably on a global basis. They must possess excellent knowledge of the pharmaceutical product development process and have broad therapeutic area exposure. In addition, a strong commercial business awareness is a must.
The candidate must have excellent communication skills with the ability to interact with senior managers and clients at all levels in order to develop key relationships.
Upon onboarding, full training will be provided however having a formal project management certification would be a plus.
Clintec (an IQVIA company), established for 22 years, is an award-winning, full-service global clinical research organisation. Our head quarter office is based in Scotland, UK and we have operations across 50+ countries worldwide.
We differ from other players in the clinical research industry as we combine the agility and flexibility typical of smaller CROs with the global coverage and management associated with large CROs.
We provide clinical research support services to clients in the pharmaceutical, biotechnology and medical device industries, assisting with key product development and managing clinical trials across all major therapeutic areas, with expertise in Oncology and Rare Disease studies.
To be considered for this role, please click the APPLY NOW button.
Alternatively if you want to know more about job opportunities at Clintec or our company, please visit our website www.clintec.com or contact our internal recruitment team directly at firstname.lastname@example.org.
Clinical Research / Clinical Trials / Clinical Research Professionals / Clinical Research Career / PM / Project Manager / Project Management