SAS Programmer in Clinical Trials

Company DescriptionWe 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 3000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those...

About Our ClientWe are looking for experienced SAS Programmers with at least 4 years of experience in the pharmaceutical industry, especially in clinical trials. If you know SAS and have experience in creating and processing data in the context of SDTM, ADaM, CDISC, TFE standards, we invite you to apply for the position of Statistical Programmer (SDTM,...

Senior Clinical ProgrammerLocation: home-based in Eastern EU (Poland, Hungary, Serbia)Why IQVIAData Sciences Staffing Solutions, DSSS or DS3, is a unit within IQVIA that provides our sponsors with fully dedicated resources through a Functional Service Provider (FSP) partnership. This means you get all the benefits of working for an industry leading CRO while...

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...

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...

About UsIQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries.We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to improve patient outcomes and population health worldwide.This role...

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....

Innovaderm is a specialized contract research organization (CRO) in dermatology.We are looking for a skilled Clinical Study Builder to join our team at TN Poland.This role involves working in a dynamic and collaborative environment to design and develop electronic case report forms (eCRFs), visit schedules, and associated data quality checks for medical...

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...

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...

About the RoleThe Site Manager is responsible for overseeing the day-to-day activities at the site under the direction of the Country Manager. This key role ensures delivery of enrollment goals while maintaining adherence to local regulations and CARE SOPs in all aspects of conducting clinical trials. The ideal candidate will have a strong background in...

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...

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...

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...

Company DescriptionWe 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 3000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those...

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 3000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.Job...

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,...