Covance Czech Rep. is looking for Clinical Project Lead! (Senior Clini
Nr ref.: /JOBS.pl
Do you demonstrate strong scientific and clinical research knowledge? Strong understanding of clinical trial planning, management and metrics? Are you able to effectively build and maintain professional relationships with investigators and other external stakeholders? Are you able to lead across several dimensions simultaneously? Do you possess knowledge of start-up and study conduct procedures? If YES you are the right person to join our Team in Prague!
We are currently recruiting experienced Senior Clinical Research Associate/Clinical Project Lead.
In this position you will have overall responsibility for the conduct of the trial in the Czech Republic, EC submissions and cooperation on RA submissions as well as development of country specific documents, site selections, co-monitoring.
About the Job:
Conducting on-site Accompanied Field Visit activities Effectively communicating management strategies, policies and procedures in conjunction with leadership teams Developing and maintaining effective relationships with client management teams Maintaining good working relationship with clients Oversees country and site validations, site selection and recruitment in assigned protocols; responsible for clinical trial education to sites
University/college degree (life science preferred), or certification in a related allied health profession In lieu of the above requirement, candidates with several years of relevant clinical research Experience in pharmaceutical or CRO industries will be considered Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements in other countries Thorough understanding of the drug development process Fluent in local office language and in English - Relevant clinical research Experience in a pharmaceutical company or CRO
ability to effectively conduct clinical studies and develop the pipeline, maintaining local regulatory and compliance requirements in countries ability to make decisions independently and oversee important activities relevant to clinical research activities in the country according to predetermined global policies and commitments with the support, strong understanding of local regulatory environment, ability to identify problems, conflicts and opportunities early and lead, communication and empathic skills ability to coordinate and lead local teams to high performance
EEO Employer Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran/Sexual Orientation/Gender Identity). Your confidentiality and privacy are important to us.