Clinical Trials Specialist

Clinical Trials Operations Specialist RoleWe are seeking a highly skilled Clinical Trials Operations Specialist to join our team. The successful candidate will have experience in managing complex end-to-end activities, working with different stakeholders and teams, and having fluency in written and spoken English. A strong background in pharmaceuticals or...

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured.We are seeking an experienced Clinical Trials Manager to join our team. In this role, you will be responsible for ensuring that clinical trials are conducted in accordance with...

The role involves working closely with the Global Program Team to manage legal risk within development programs. Key responsibilities include providing pragmatic, solutions-oriented legal advice to colleagues across all levels of the organization. Additionally, the successful candidate will participate in Legal Department projects and initiatives, as well as...

At Comac Medical, we are seeking a talented Clinical Research Associate to join our team. As a critical member of our clinical research department, you will be responsible for ensuring the success of our clinical trials.Key ResponsibilitiesThe successful candidate will be responsible for developing and maintaining strong relationships with sites...

Role SummaryThis is a full-time position as a Clinical Trials Coordinator, requiring a College/University degree in Life Sciences or an equivalent combination of education, training, and experience. The ideal candidate should have minimum 2 years of experience in independent on-site monitoring in Poland and full working proficiency in Polish, English, and MS...

At PSI CRO, we are dedicated to delivering high-quality services in clinical trials. As a Clinical Trials Data Scientist, you will play a vital role in our team by working with patient and operational data, developing new data solutions, and setting up Risk-based Monitoring systems.About the RoleYou will participate in the selection of the Risk-Based...

We are seeking an experienced Clinical Data Science Specialist to join our Clinical Trials team at PSI CRO. As a key member of our team, you will be responsible for developing and implementing data science solutions to support our clinical trials operations.About the RoleDevelop and implement data science solutions to support our clinical trials...

Syneos Health, Inc. is a fully integrated biopharmaceutical solutions organization built to accelerate customer success.We are seeking a seasoned Senior Director of Clinical Trials to provide overall strategy and direction of clinical trials, processes and procedures.This role involves acting as a primary senior-level contact for customers and participating...

About UsRho, Inc. is a full-service Contract Research Organization (CRO) based in North America.We offer a comprehensive benefits package for all benefit-eligible employees and encourage a work-life balance that allows employees to bring their best selves to work.Job Title: Freelance Clinical Project ManagerMain ResponsibilitiesManage international clinical...

Job DescriptionRho, Inc. is a leading Contract Research Organization (CRO) with a global presence.We are seeking a highly experienced Freelance Clinical Project Manager to join our team in the EU, working on a freelance basis to manage international Phase I-IV clinical trials.Main DutiesManage clinical studies from start to finish, ensuring compliance with...

Job Title: Clinical Trials Proposal ManagerClinical Trials Proposal Manager will coordinate all phases of PSI's proposal process, maintaining the company's win rate of 30% and higher. The ideal candidate will contribute to RFP strategy, bid defense slide decks, and partner with global teams of subject matter experts from various departments.Key...

Job DescriptionWe are seeking an experienced Clinical Research Associate to join our team at August Research. The successful candidate will be responsible for:Site identification and selectionRegulatory submissionsMonitoring for clinical studiesLocal safety reportingThis is a full-time position for candidates with at least one year of monitoring experience....

Role OverviewPrimeVigilance Ltd is seeking a dedicated Medical Case Reviewer to join our team. The successful candidate will be responsible for reviewing individual case safety reports to ensure compliance with regulatory requirements and client expectations.About the Job:Reviewing individual case safety reports from various sources (clinical trials,...

About the RoleWe are looking for an experienced Data Scientist in Clinical Trials to join our team at PSI CRO AG. As a key member of our Central Monitoring department, you will be responsible for developing and implementing data solutions using advanced analytics.Main Responsibilities:Collaborate cross-functionally to identify study challenges and develop...

About the RoleWe are seeking a highly skilled Clinical Documentation Specialist to join our team at IQVIA. As a key member of our organization, you will be responsible for ensuring the efficient and effective management of Trial Master Files (TMFs) and other related documents.Main ResponsibilitiesDrive TMF quality at the trial level by acting as a single...

TN Poland is a leading clinical research organization seeking a highly skilled Clinical Contract Specialist to join their team.Job DescriptionThe successful candidate will be responsible for developing, negotiating, and finalizing site agreements and budgets for medical device clinical trials across various therapeutic areas. They will collaborate with...

Company OverviewPSI CRO is a dynamic, global company founded in 1995. We bring together over 3000 driven individuals who are passionate about medical science and changing lives.Job DescriptionThe Clinical Data Scientist will work with clinical trials patient and operational data, develop new data solutions, and set up Risk-based Monitoring systems in the...

At ICON plc, a world-leading healthcare intelligence and clinical research organization, we're seeking a highly skilled Pharmacovigilance Assistant to join our dynamic team in Warsaw.This role plays a vital part in supporting the collection, documentation, and reporting of safety data related to medications and clinical trials. As a Pharmacovigilance...

Clinical Data ManagerAs a Clinical Data Manager at Hays Poland, you will be responsible for leading the planning and execution of data management methodologies for assigned clinical studies.You will collaborate with study teams to implement data management strategies and practices that ensure high-quality data delivery.Key responsibilities include designing...

Company OverviewCare Access is a pioneering force in the clinical research sector, fostering collaboration among physician investigators, nurse coordinators, and operations managers. Our mission revolves around making clinical trials an accessible care option for every patient.