Clinical Study Associate

**Job Title:** Clinical Study Specialist**About the Role:**The Clinical Study Specialist provides technical and administrative support to clinical study teams responsible for clinical trial execution. This role involves working on the execution of one or more studies across a program, receiving assignments from the Clinical Study Lead or Clinical Study...

The Clinical Study Specialist (CSS) provides technical and administrative support to the clinical study team(s) responsible for clinical trial execution. The CSS may be assigned to support the execution of one or more studies across a program. The CSS receives assignments from the Clinical Study Lead or Clinical Study Associate Manager. The CSS will support...

The Clinical Study Specialist (CSS) provides technical and administrative support to the clinical study team(s) responsible for clinical trial execution. The CSS may be assigned to support the execution of one or more studies across a program. The CSS receives assignments from the Clinical Study Lead or Clinical Study Associate Manager. The CSS will support...

The Clinical Study Specialist (CSS) provides technical and administrative support to the clinical study team(s) responsible for clinical trial execution. The CSS may be assigned to support the execution of one or more studies across a program. The CSS receives assignments from the Clinical Study Lead or Clinical Study Associate Manager. The CSS will support...

About the RoleWe are seeking a highly skilled Clinical Study Specialist to join our team. As a Clinical Study Specialist, you will provide technical and administrative support to the clinical study team responsible for clinical trial execution.

25 GBP - 25 GBP - Uxbridge, United Kingdom - Contract **Freelance Clinical Trial Associate Opportunity with Leading Global Pharma - UK Based** **Company Overview**: Join a dynamic and innovative global pharmaceutical company committed to advancing healthcare through groundbreaking research and development. We are seeking a highly motivated and experienced...

The Clinical Study Specialist (CSS) provides technical and administrative support to the clinical study team(s) responsible for clinical trial execution. The CSS may be assigned to support the execution of one or more studies across a program. The CSS receives assignments from the Clinical Study Lead or Clinical Study Associate Manager. The CSS will support...

Job Title: Clinical Study SpecialistAbout the Role:We are seeking a highly skilled Clinical Study Specialist to join our team at Pharmiweb. This is a unique opportunity for an experienced professional to take on a challenging role in clinical operations.

Estimated Salary: $120,000 - $180,000 per yearGilead Sciences is a leading biopharmaceutical company dedicated to creating life-changing scientific innovations. As a Clinical Study Director, you will play a critical role in the execution of Phase I - IV clinical trials across all therapeutic areas.Key Responsibilities:Manage study logistics and define...

Job OverviewClinical study team support is a key component of Regeneron's research and development efforts. We are seeking a skilled Clinical Study Specialist to provide technical and administrative assistance to our clinical study teams. This role requires strong organizational skills, attention to detail, and effective communication abilities.Salary...

**Working with Us** Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...

Job DescriptionClinical Study Specialists at Regeneron are responsible for providing technical and administrative support to the clinical study team responsible for clinical trial execution. This position requires strong attention to detail, excellent communication skills, and the ability to work effectively in a team environment.About the CompanyRegeneron...

**We are currently looking for an Initiation Clinical Research Associate II to join our UK Clinical Study Start-Up Team in Uxbridge.** The **Initiation Clinical Research Associate **(**iCRA**) specializes in performing all study start up activities for a clinical trial. You will participate in Pre SIV activities and be assigned & accountable for managing...

About the RoleWe are seeking an experienced Clinical Project Manager to lead our global clinical trials operations team. As a key member of the Clinical Operations group, you will play a critical role in ensuring the success of our clinical trials by defining and implementing effective study logistics and clinical study plans.Your primary responsibilities...

**Job Summary:**We are seeking an experienced Associate Director to join our clinical data management team at Regeneron Pharmaceuticals, Inc. This role will be responsible for leading clinical data management activities across programs and ensuring the delivery of high-quality results.Key Responsibilities:Act as point of contact for clinical program and...

The Senior Clinical Study Lead (CSL) is expected to operate with high-degree of independence and is accountable for the global execution of assigned large and/or complex clinical trials from study design, through execution, to study close out. The Senior CSL is accountable for the study timelines, study budget, and ensuring study conduct is in accordance...

The Senior Clinical Study Lead (CSL) is expected to operate with high-degree of independence and is accountable for the global execution of assigned large and/or complex clinical trials from study design, through execution, to study close out. The Senior CSL is accountable for the study timelines, study budget, and ensuring study conduct is in accordance...

For Current Gilead Employees and Contractors: Please log onto your Internal Career Site **Job Description**: Gilead has declared Oncology as one of the key therapeutic areas for future growth. Gilead is growing its pipeline in immune oncology through internal research, partnerships and acquisitions. The Clinical Operations team is responsible for the...

Gilead Sciences is continuing to hire for all open roles. Our interview process may be conducted virtually and some roles will be asked to temporarily work from home. Over the coming weeks and months, we will be implementing a phased approach to bringing employees back to site to ensure the health and safety of our teams. **For Current Gilead Employees and...

About the Role:The Associate Director, Program Clinical Data Management Lead is a key position in our organization, responsible for leading and managing programs in Clinical Data Management (CDM). This role requires a minimum of 12 years of experience in the biotechnology, pharmaceutical, or health-related industry, with a strong background in CDM.As a...