Clinical Trials Data Strategist

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...

**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 &...

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 plus years of...

Manages all clinical operational and quality aspects of allocated studies, of low to  moderate complexity, in compliance with ICH GCP. In accordance to project  specific requirements, may assume Clinical Study Manager (CSM) responsibilities  on small and/or less complex projects. Develops clinical tools ( Monitoring Plan, Monitoring Guidelines)...

**Description** **Medical Writer II** Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide practical value to help our customers...

**Description** **S**r CMA I** Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide practical value to help our customers...

Job Description  Our client, a world leader in Pharmaceuticals & In vitro diagnostics (IVD), is looking for a "Clinical Development Lead" for their Infection and Immunity department. The team is dedicated to providing clinical guidance and developing new laboratory and digital diagnostic products in the areas of infectious diseases and immunology. They...

**Payroll**- Direct **Knowledge part**: Thorough knowledge of ICH - GCP, New Drugs and Clinical Trials rule 2019 and updating self from time to time on Regulatory and process changes (if any). Action part: P.I. Coordination, Patients screening, randomization, source documentation, site master file maintenance, eCRF entry, PK/ ADA sample collection,...

Job Description Our client, a world leader in diagnostics and life sciences, is looking for a "Clinical Supplier Relationship Manager (100% Remote)" .Duration: Long Term Contract (Possibility Of Further Extension) This job requires a combination of advanced skills and experience in identifying, selecting and managing external suppliers of Clinical Trial...

Data Scientist (Pharma Industry) - 4+ Years Experience Key Responsibilities: Develop and implement data models and algorithms to analyze large datasets from various sources. Collaborate with cross-functional teams to design and execute data-driven solutions for drug development and clinical trials. Utilize machine learning and statistical techniques to...

Clinical SAS Programmer (India) India CRO - Biometrics Full-time The Clinical SAS Programmer will lead the programming activities for various purposes including SAS Data Listings to be used for data review, Safety Review Listings, Centralized Monitoring Listings and Reports. The Clinical SAS Programmer will also be responsible for...

Description Job Description: Senior Business Analyst with Clinical Data Management Experience We are currently seeking a highly skilled and experienced Business Analyst with a strong background in clinical data management to join our team at Saama. This role is ideal for someone who is passionate about leveraging their expertise in clinical data...

Global Life Science Hub is currently representing a reputable mid-size CRO known for its extensive experience and expertise in providing a wide range of services to the life science industry. This CRO, with a strong track record of delivering high-quality solutions, is seeking an experienced Contract Data Manager. Responsibilities : Collaborating closely...

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The Principal Statistical Programmer is responsible for creating programs to develop, validate, and document datasets, tables, listings, and figures related to the compounds being studied. The focus for this position will be on support of clinical development and post-marketing activities. Programming expertise is needed for data review and to support...

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