We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.
PSI’s business is about conducting clinical research of novel medications. We work at the interface of R&D, pharmaceutical industry and healthcare science and provide services to big and mid-sized pharmaceutical companies. We help our clients to generate data about safety and efficacy of medications and bring the best ones to market. By conducting global clinical research trials, PSI makes cutting-edge treatment available in drugstores all over the world and helps patients with serious medical conditions to improve or even save their life. Help us to make sure that PSI medical and business documents are clear to patients, physicians, regulatory authorities, and clients.
We offer an inspiring story of the company that has grown organically from a handful of countries to global presence. PSI is a mature company with standards and practices, but we do not stand still. Every day, there is a figurative Everest to climb, and you will not get bored here.
Job DescriptionTake your career to the next level and lead challenging study activation process on a country/regional level. You will support clinical research teams and ensure PSI projects start smoothly and on time.
Office based in Taipei
You will:
Perform administrative activities related to the clinical study startup process in Taiwan: documents collection/distribution to hospitals, translation of startup documents, filing, database (CTMS) maintenance, minutes keepingProvide regular site startup progress updates to project teamsCoordinate preparation of initial submission dossiers to competent authorities, ethics committees, and/or site submission dossiersPrepare IP-RED packagesMonitor startup key performance indicators for the assigned projectsQualificationsCollege or University degree or an equivalent combination of education and experience that provides the individual with the required knowledge, skills, and abilitiesMinimum of 1 year industry experience in clinical research in an administrative roleExcellent knowledge of FDA guidelines and ICH GCPCommunication and interpersonal skillsAttention to detailAbility to work in a team or independentlyAdditional InformationMake the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.
PSI is an inclusive and equal opportunity employer and is committed to attracting and retaining a diverse workforce that reflects the community we serve.