Clinical Data Standard Specialist

The Aixial Group is an International Contract Research Organization (CRO), a member of the ALTEN Group, providing complex services in clinical trials (phase I-IV) and non-interventional studies. Our offices are located in France, Belgium, Switzerland, Germany, Denmark, Sweden, UK, Romania, US, India and Czech Republic.The CRO occupies a unique position in...

We are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow. Who are we? A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence 20+ years of...

We are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow. Who are we? A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence 20+ years of...

We are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow. Who are we? A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence 20+ years of...

We are expanding We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow. Who are we? A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence 20+ years of...

We are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow. Who are we? A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence 20+ years of...

We are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow. Who are we? A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence 20+ years of...

We are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow. Who are we? A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence 20+ years of...

We are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow. Who are we? A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence 20+ years of...

We are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow. Who are we? A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence 20+ years of...

About Noccarc: Noccarc specializes in designing and manufacturing of Smart Medical Devices and an integrated Digital Platform for ICUs, revolutionizing ICU operations and management. Our devices adhere to international standards such as US-FDA and CE guidelines, competing strongly with top international products. With over 9 patents, our dynamic in-house...

Position Summary: The Clinical Data Manager/Senior Clinical Data Manager is responsible and manages all aspects of the clinical trial data management process from study start up to post database lock for assigned projects. Standard Operating Procedures / Work Instructions (SOPs/WIs); regulatory directives; study specific plans and guidelines will be...

Clinical/DRG Validation Specialist We are recruiting experienced, certified senior Clinical/DRG Validation Specialists with extensive knowledge of ICD-10-CM and PCS coding, current proficiency in coding clinics, and excellent communication skills. Qualifications: Minimum of 2-4 years of experience in Clinical Validations and at least 5 years in Inpatient...

**Job Code**:SE / MDC / 00615**Job Location**:Multiple Cities / Hybrid / Remote**Experience**:3 - 5 yrs**Skills Required**: - Bachelor’s degree or equivalent, preferably in Health Sciences. - 3 years’ relevant experience in Clinical Data Coding. - In‐depth knowledge of industry standard coding (MedDRA, WHO Drug) - Experience working on clinical...

**Brief Position Description**: The core responsibility for this position is as a member of the Data Management department at Novotech. The Clinical Data Programmer-II (CDP-II) will be responsible for programming activities on clinical trial projects and to ensure compliance with Good Clinical Data Management Practices (GCDMP). **Minimum Qualifications &...

Brief Position Description:The core responsibility for this position is as a member of the Data Management department at Novotech. The Clinical Data Programmer-II (CDP-II) will be responsible for programming activities on clinical trial projects and to ensure compliance with Good Clinical Data Management Practices (GCDMP).Minimum Qualifications &...

Job Code:SE / MDC / 00615Job Location:Multiple Cities / Hybrid / RemoteExperience: 5 yrsSkills Required:Bachelor's degree or equivalent, preferably in Health Sciences. 3 years' relevant experience in Clinical Data Coding. In‐depth knowledge of industry standard coding (MedDRA, WHO Drug) Experience working on clinical trials. Working knowledge of GCP/ICH...

Minimum Qualifications & Experience: Graduate in a clinical or life sciences related field. Relevant experience /qualifications in allied professions may also be considered. At least two to four years data management experience working in research, pharmaceutical industry, or a related field. **Responsibilities**: Member of the project team reporting to the...

Minimum Qualifications & Experience:Graduate in a clinical or life sciences related field. Relevant experience /qualifications in allied professions may also be considered. At least two to four years data management experience working in research, pharmaceutical industry, or a related field.Responsibilities:Member of the project team reporting to the...

**Brief Position Description**: Brief Position Description: The Clinical System Liaison plays a pivotal role in the Clinical Research Organization (CRO), liaising between technology (clinical systems) and clinical research operations. This role involves in facilitating the effective utilization of data in clinical systems and reporting platforms for...