study submission

Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical...

One of our prestigious publisher clients is looking for project-based Managing Editors support to ensure timely, high‑quality editorial decisions across a portfolio of journals. In this role, candidates will need to make independent, post–peer review decisions, uphold journal standards, and collaborate closely with internal teams to maintain throughput...

DescriptionFreelance opportunity in Greece! Interested to join our Clinical Operations team as a Senior Start Up Associate (SSU) with regulatory and start up experience in Greece for 0.5 FTE? Senior Start Up Associate is responsible for managing study start-up activities at country and sites’ levels under CTR via CTIS for Part 2 and as per other...

Job OverviewPerform 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.Essential Functions• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with...

Job OverviewPerform 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.Essential Functions• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Country Approval Specialist – Make an Impact at the Forefront of Innovation!As part of our global team, you’ll have the opportunity to participate in the management and preparation, review, and coordination of Country Submissions in line with the global submission...

About the RoleWe are looking for a detail -οriented and proactive Regulatory Affairs & CMC Officer to join our team. In this role, you will play a key part in ensuring the regulatory compliance of our pharmaceutical products across the EU and Rest of World (RoW) markets.  You will collaborate closely with...

  Work Your Magic with us!     Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for...

  Work Your Magic with us!     Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for...

  Work Your Magic with us!     Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for...

Description#One Group | One PowerWe are Enerwave, member of HELLENiQ ENERGY and a leader in providing outstanding and innovative energy solutions. We operate with passion, being engaged in heart and mind to what we do, and we pride ourselves on offering our employees a place where they can excel, creating value. We are offering now a set of exciting...

To meet current corporate needs, we would like to bring to our team a Permitting Senior Associate Based @ The Ellinikon Offices We are seeking a highly motivated Permitting Senior Associate to join the Urban Planning and Permitting Department. The Permitting Senior Associate will be reporting to the Permitting Senior Manager. The Successful Candidate...

Sponsor Dedicated - Sr Medical Writer (CSR, Protocols, IB and Reg documents)Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and...

DescriptionPLANET S.A. is looking for enthusiastic and skilled senior IT Project Manager, demonstrating a high level of technical competency and independence, as well as experience and ability in managing complex environments. Responsibilities: Participate in the management of various projects enterprise architecture design in the fields of IT ...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as an Assistant Clinical Research Associate – Make an Impact at the Forefront of Innovation!We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.As part of our...

DescriptionFor a leading Greek pharmaceutical company. ResponsibilitiesLead and coordinate R&D projects, ensuring timely delivery within scope, budget, and quality requirements.Collaborate with cross-functional teams (R&D, Regulatory Affairs, Supply Chain, Quality, and external partners) to support successful project execution.Develop, monitor, and maintain...

PharmaPath, a Greek pharmaceutical company with a rich history and significant legacy in the pharmaceutical field of generic medicines, is seeking a dedicated and skilled Project Management Supervisor to join our dynamic team. Main duties and responsibilities:Lead and coordinate R&D projects, ensuring timely delivery within scope, budget, and quality...

DescriptionQA Operations Officer (Ref: QAO_0225) About the companyRAFARM is an innovation-driven, dynamically growing pharmaceutical company and a well-established European manufacturer with an outward-looking orientation that invests 13% of net turnover in Research and Development. We introduce high technology in our state-of-the-art sterile manufacturing...

For a leading Greek pharmaceutical company. Responsibilities • Lead and coordinate R&D projects, ensuring timely delivery within scope, budget, and quality requirements. • Collaborate with cross-functional teams (R&D, Regulatory Affairs, Supply Chain, Quality, and external partners) to support successful project execution. • Develop, monitor, and...

Description As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides an opportunity for all employees to collaborate internationally, offering visibility and the opportunity to directly contribute to the company's success. We...