Project Manager/Senior Project Manager – Clinical (Oncology/CNS/Rare Disease) in Bucuresti

Bucharest, Romania Are you an experienced clinical trial Project Manager who’s engaged in addressing the challenges facing the research and development of novel compounds in Oncology, Rare Disease or CNS? Are you passionate about impacting the health and lives of patients around the world? Do you take a consultative approach to trial management, proving to be a valuable partner in trial operational delivery?Precision for Medicine (CRO) are looking for experienced Project Managers with ideally experience in ONCOLOGY and/or RARE DISEASES or CNS who have managed full service clinical projects within a CRO/Pharmaceutical setting. We can offer a Project Manager or Senior level position depending on experience.This is a remote based position in Europe. We are flexible to consider any European location where PFM have a legal entity, including: UK, Spain, France, Germany, Italy, Poland, Hungary, Romania, Slovakia, Serbia, Belgium or Netherlands.In this pivotal role you will have full service oversight for clinical projects across global/regional (ph I-IV) trials, within Oncology (or Rare Diseases or CNS). Accountable for clinical project delivery, oversight of all departments, and ensuring agreed timelines, scope, cost and quality.Involved in all study stages, including proposal strategy, development, costing, and bid defence, and seeing studies through the full cycle to completion, managing the client relationship, project team and budget and timelines throughout. You will work in a cross-functional team with both internal and external stakeholders, driving quality and coordinating the study team.Precision for Medicine is a precision medicine CRO. Our uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical authorities, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology.We invite you to learn more about our growing organization serving our clients that are researching ground-breaking cancer therapies. We strive to ensure employees feel appreciated for the contributions they make every single day.You will independently lead clinical programs in accordance with the study budget and scope of work. You will use your strong interpersonal and organizational skills to set and achieve objectives in the execution of the programs; both contracted objectives and financial objectives. You may be called upon to run international trials as well.We offer an amazing high-energy, dedicated, collaborative team members who enjoy a challenge, thrive in the details and flourish in dynamic environments. If you are no stranger to taking charge and seek positive teamwork to deliver extraordinary work, we have an opportunity for you.How we will keep you busy and support your growth: Serve as the primary point-of-contact liaison with the client to provide excellent customer service, including participation in proposal activities and client presentationsLiaise with Project Team and senior management of both Precision and sponsors, including C levelHandle and lead all aspects of a clinical research trial or trialsTotal project management for all functional areas including data management, safety, clinical, medical monitoring and biostatistics, etc.Prepare project status updates for clients and management; identifying key deliverables and performance metrics of success and escalation.Serve as an active member of the Project Team with the goal to contribute towards efficient management and execution of trialsPrepare and reviews protocols and other study documentation such as project plans, inform consents, site contracts and budgets Requirements: Degree or similar related life science qualification, or equivalent combination of education and experience.Previous experience in a full service Clinical Project Management role is essential.5/7+ years of clinical trial experience in pharmaceutical, biotech or CROWorking understanding of GCP/ICH guidelines and the clinical development processAbility to drive and availability for domestic and international travel including overnight staysProven computer skills (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, EDC, IXRS)Proven ability to develop positive working relationships with individual and teams internally and externallyDemonstrated core understanding of medical terminology and clinical trial activities as it relates to the execution of a clinical development plan Preferred: Masters programs with concentration in a scientific or healthcare disciplineUnderstanding of financial management, shown ability to identify changes in scope and successfully address those changes appropriately Any data provided as a part of this application will be stored in accordance with our .Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. © 2020 Precision Medicine Group, LLCIf you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at . To help us track our recruitment effort, please indicate in your cover/motivation letter where (vacanciesinukraine.com) you saw this job posting.