Associate Director, Clinical Process Management

392967BR **Associate Director, Development Unit Clinical Quality Assurance**: Spain **About the role** **Location**: Barcelona or Madrid (Hybrid) You will be joining a team of 40 highly talented CQA professionals who are based in various countries across the globe! As our Associate Director, Development Unit CQA (Clinical QA) Program Lead, you will...

**Director Clinical Data Management** **Hybrid work (3days from the office, 2 days from home)** The role holder will be responsible for developing the Clinical Data Management (CDM) strategy for either the therapeutic area/indication and/or strategic roles at DM organisation level. Will be responsible for CDM quality, management of external partners,...

.(Role description) At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you're our kind of person. At...

**Location: Barcelona (on-site)** Join us as an Associate Director, Business Process Owner in our Biopharmaceuticals R&D department. In this role, you will work collaboratively with Functional Process and Subject Matter Experts across all relevant departments of the DevOps organization. Your primary goal will be to ensure that the processes developed and...

**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office **Position Overview** The Associate Director, Clinical Development Science provides clinical development expertise into a multi-disciplinary team engaged in advising clients in early through late-stage development of medical products. Inpout will be provided into the design and...

[Role description] At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you're our kind of person. At...

.[Role description]At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you're our kind of person. At...

The **Associate** **Director, Document Management **is a member of the Business Process Management and Optimisation (BPMO) Document Managers team, and is responsible for control, security, accessibility, development and timely delivery of process related documents for the clinical business processes owned by BPMO. As part of this role Associate Director,...

**Location: Barcelona**: Join our Biopharmaceuticals R&D team as an Associate Director, Study Management. In this role, you will provide oversight for Study Supply Management activities, ensuring delivery across a breadth of supply functions within the LCS (Logistics and Clinical Supply) matrix. You will independently plan, handle and deliver all aspects of...

(Role description) At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you’re our kind of person....

Role holders provide strategic leadership and communications expertise to clinical drug programs. They author clinical-regulatory documents and provide critical review to achieve high quality standards. They represent the skill on drug and non-drug projects. **Typical Accountabilities** The Clinical Regulatory Writing team provides expert communications...

When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform to connect, work at pace and challenge perceptions. That’s why we work, on average, a minimum of three days per week from the office. But that doesn’t mean we’re not flexible. We balance the...

.Job Description Summary Associate Director, Clinical QA Program Lead (m/f/d) Location: Barcelona Gran Vía, Spain #LI-Hybrid The Associate Director, Clinical QA Program Lead will provide Quality oversight for the end-to-end clinical process for the clinical trials under responsibility to ensure compliance with the Health Authorities requirements, the...

Job Overview:We are looking for an Associate Director of Clinical Operations to join our team at Amgen Inc. (IR) in Barcelona, Spain.Key Responsibilities:Lead the negotiation of site contracts and budgets.Develop and implement strategies to improve the contracting process.Collaborate with cross-functional teams to resolve contract and budget issues.What...

.Job Description Summary As our Clinical Development Medical Director in our Immunology Development Unit you will be responsible for the scientific and clinical strategy of assigned clinical trials, scientific monitoring, and reporting of quality data. Job Description The Clinical Development Medical Director (CDMD) for Rheumatology is the clinical leader of...

**About AstraZeneca** AstraZeneca is a global, innovation-driven BioPharmaceutical business that focuses on the discovery, development and commercialisation of prescription medicines for some of the world’s most serious disease. But we’re more than one of the world’s leading pharmaceutical companies. At AstraZeneca we’re dedicated to being a Great...

Unlock a Career in Clinical ResearchSyneos Health is a leading biopharmaceutical solutions organization, accelerating customer success through innovative clinical development models. As a Clinical Research Associate II at Syneos Health, you will be part of a dynamic team that simplifies and streamlines work to make the company easier to work with and...

**Location: Barcelona, Spain (On-site): We requiere 3 days working from the office and 2 days working from home.**: Join our Biopharmaceuticals R&D team as an Associate Director, Study Management. In this role, you will provide oversight for Study Supply Management activities, ensuring delivery across a breadth of supply functions within the LCS (Logistics...

Job Description Summary Associate Director, Clinical QA Program Lead (m/f/d)Location: Barcelona Gran Vía, Spain #LI-HybridThe Associate Director, Clinical QA Program Lead will provide Quality oversight for the end-to-end clinical process for the clinical trials under responsibility to ensure compliance with the Health Authorities requirements, the internal...

Job Description Summary Associate Director, Clinical QA Program Lead (m/f/d) Location: Barcelona Gran Vía, Spain #LI-Hybrid The Associate Director, Clinical QA Program Lead will provide Quality oversight for the end-to-end clinical process for the clinical trials under responsibility to ensure compliance with the Health Authorities requirements, the...