Global Study Associate

Global Study Manager is a member of extended global study team supporting delivery of clinical studies within Global Medicines Development (GMD) to time, cost and quality, from Clinical Study Protocol (CSP) development through study set-up, maintenance, close-out, development of Clinical Study Report (CSR) to study archiving. The GSM works...

Locations: Barcelona, Spain (on-site) Warsaw, Poland (on-site) Mississauga, Canada (on-site) The Global Study Director (GSD) is a business-critical role within Study Management, BioPharmaceuticals Clinical Operations, whose main accountability is the operational planning and delivery of high priority and complex clinical studies or multiple...

Global Study Manager is a member of extended global study team supporting delivery of clinical studies within Global Medicines Development (GMD) to time, cost and quality, from Clinical Study Protocol (CSP) development through study set-up, maintenance, close-out, development of Clinical Study Report (CSR) to study archiving. The GSM works...

We are currently recruiting for the position of Associate Clinical Trial Manager in Poland for a global leader in the diagnostic and medical industry. The person in this role will be part of the Clinical Trials Team, responsible for the planning, execution, management, and closure of projects related to the company's clinical trial plans. A key part of the...

We are currently recruiting for a Clinical Trial Associate for a global leader in diagnostics/medical industry. This position is responsible for assisting in the execution of clinical trials by providing quality administrative and project management support. If you already have at least one year of experience in clinical trials and have advanced English...

The Associate Project Manager ensures the successful initiation, planning, execution, monitoring, controlling and closure of assigned clinical research projects. The Associate Project Manager must ensure compliance with the study budget, project scope and timelines and in accordance with applicable standard operating procedures (SOPs), good clinical...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations...

Associate Site Manager with French Real-World Evidence Hybrid: EMEA Join us on our exciting journey! IQVIA Real-World Evidence (RWE) teams work with clients to help them collect and use real-world data to generate evidence to meet the needs of regulators, payers, providers, and patients. Our approach is unique in the industry and is defining the...

The position As Clinical Research Associate your role is to verify the accuracy and completeness of the trial data, that the rights and well-being of human subjects are protected, and the conduct of the trial follows the current approved protocol, GCP and local legislations. As a CRA, you will be representing Novo Nordisk and being the main point of...

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond...

Job DescriptionThe Global Rewards Associate in is a core enabler of the Rewards and Recognition strategy of Docplanner. The role guarantees diligent, relentless execution of the compensation strategy at global level, and contributes to the results, engagement and competitiveness of Docplanner. You will create value by: Building and maintaining a global...

Description of Services) • Co-ordinate/manage timely contributions of AZ core/extended members • Interface with key stakeholders cross-functionally, and/or external partners, to identify, manage and resolve issues affecting study delivery • Review protocol drafts and input operational perspectives/content into document and authoring team...

We are the largest digital healthcare platform in the world, present in 15 countries and currently connecting over 30 million patients to more than 2 million healthcare professionals. We seek to make the experience in health more human and we live and breath this mission.We obsess over the challenge of minimizing patients' pain and helping healthcare...

Location : Warsaw (PL) Salary: Competitive, with excellent benefits. Hybrid model of work : 3 days in office, 2 days remote per week This role sits within the Clinical Document Anonymisation and Data Sharing function in Clinical Trial Transparency, Chief Medical Office. The Clinical Trial Transparency leads the AstraZeneca Group of Companies,...

Life Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living. At Smith+Nephew we are looking for: Senior Associate, Global Customer Care, Poland What will you be doing? Manage incoming customer orders (sales, consignment, loan) and ensure timely processing and delivery Enter orders into the SAP system and...

Clinical Research Associate II, Poland (dermatology and rheumatology CRO)The Clinical Research Associate II (CRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all...

IQVIA is hiring Clinical Research Associates! Join IQVIA today and make an impact on patients’ outcome! Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. ...

If you enjoy partnering with contacts across the firm, building strong relationships with your colleagues and helping to move the business forward while helping comply to our regulatory commitments and associated policies, this could be the position for you. Corporate Third Party Oversight (CTPO) Legal Entity Broker is a centralized group within Global...

Job Description The Role We are currently seeking candidates for the position of Associate in our Global Financial Markets department. Up to four positions are available at the moment. Who are we looking for? The firm's offer is primarily addressed to law graduates and persons in the first or second year of their legal training, but we will also...

ADI Global Distribution now have the opportunity for a Associate Category Manager to join our Category Management team based in Warsaw, Poland and report to our EMEA Head Office in managers based in UK. This role is hybrid working with 3 days working from the office and 2 days from home.  ADI Global, a division of Resideo Security Group, is seeking an...