The Center for Catastrophe Modeling and Resilience at Lehigh University seeks a motivated and talented Postdoctoral Research Associate to contribute to our research initiatives and academic programs. This role offers a unique opportunity to work with Professor Rahnemoonfar in
Senior Clinical Research Associate ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the
Base level role Perform comprehensive data management tasks including data review, query generation and query resolution. This may also include, but is not limited to creation of eCRF completion guidelines, entry of test data for eCRF and the Data Review
Job Overview Provide project related assistance to assigned project teams.; Ensure all work is conducted in accordance with standard operating procedures, policies, good clinical practices and applicable regulatory requirements.; Meeting quality and timeline metrics. Essential Functions
About the Team ShopriteX was established to accelerate the use of data to improve customer experience and business operations. Our Agile way of working allows for flexibility to grasp new opportunities and quickly transform them into insights
Do you have expertise in, and passion for Brand Management and Oncology? Then AstraZeneca might be the one for you! ABOUT ASTRAZENECA AstraZeneca is a global, science-led, patient-focused biopharmaceutical business that discovers, develops, and commercialises prescription
The successful candidate will be responsible for the following key performance areas: Provide input regarding the issuing and/or amending of interoperable, operator and scheme rules. Review and process the applications for exemptions and other legislative, regulatory
The successful candidate will be responsible for the following key performance areas: Review and process licensing applications (designations, registrations, licensing and authorisations). Review and provide initial input into licensing and authorisation legislation and frameworks of the
Lehigh Universitys Office of International Affairs (OIA) is seeking a tech savvy, detail-oriented, culturally sensitive and collaborative administrative professional to support one of its most student-facing units. This is an opportunity to contribute meaningfully to international
Job Title: Authorizations Specialist Location: South Africa Job Type: Full-Time, Remote Working Hours: US Hours (9am-5pm EST) Salary: South African Rand (ZAR) About the Role We are seeking a detail-oriented and proactive Authorizations Specialist to join
Job Overview Provides leadership of the centralized monitoring team, in partnership with project and clinical lead, and in collaboration with other functional teams, to achieve the delivery of the project’s overall objectives to the sponsor’s satisfaction
At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where ,Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with
Are you looking to join a company where your contributions truly matter, and where youll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great
Job Title: Medical Administrator Location: South Africa Job Type: Full-Time, Remote Working Hours: US Hours (9am-5pm EST) Salary: South African Rand (ZAR) About the Role We are seeking a detail-oriented and proactive Medical Administrator to join
The Clinical Research Associate II (CRA II) manages clinical study sites and monitors site activities to assure adherence to Good Clinical Practices (GCPs), Standard Operating Procedures (SOPs), study protocols, and applicable regulatory requirements. Reviews regulatory documents as required
Production Research Associate Reference: PTA -EV-1 An established agrochemical manufacturer is seeking a Production Research Associate to conduct field agronomy research and production research field trials by assisting with regional and global Production Research technology projects, ensuring operational excellence and driving continuous improvement
Overview UNU-WIDER is hiring a Research Associate in Pretoria, South Africa. As Research Associate you would contribute to the data lab management and research for our Southern Africa – Towards Inclusive Economic Development (SA-TIED) programme which builds critical bridges between research and policy
Develop and integrate new features to enhance functionality in our products and models for internal and external users Champion best practices in software development within the team Write comprehensive tests and documentation to ensure reliability Create
Research Associate - Pretoria, South Africa UNU-WIDER is looking for an outstanding individual with strong commitment and potential to support the research programme of the Institute. Closing date: 27 October 2017, 23:59 UTC+3. United Nations University objectives The United
Role Summary The Clinical Quality Associate Director (CQAD) is responsible for maintaining, developing, and communicating high‑quality standards in the delivery of clinical studies. The CQAD plays a central role in coordinating and meeting the training needs of