
Clinical Trial Data Integrity Specialist
12 hours ago
The Central Data Quality Specialist plays a pivotal role in ensuring the quality and integrity of clinical trial data through centralized monitoring activities, statistical data review, and proactive risk management.
This critical position is responsible for developing Risk-Based Quality Management (RBQM) plans and conducting thorough study risk assessments to identify potential issues and develop mitigation strategies.
Key responsibilities include:
- Developing comprehensive RBQM plans to ensure high-quality data collection and analysis.
- Conducting thorough study risk assessments to identify potential issues and develop mitigation strategies.
- Performing centralized statistical monitoring and data analysis on study data to detect anomalies, trends, and potential risks.
- Collaborating with cross-functional teams to ensure seamless data cleaning and oversight processes.
Requirements include:
- Bachelor's Degree in a relevant field or equivalent combination of education and experience.
- Minimum 2 years experience in clinical monitoring, clinical trial management, or a related field.
- Working knowledge of ICH GCP guidelines and the clinical development process.
Skills required include:
- Statistical analysis and data monitoring.
- Risk assessment and mitigation.
- Report writing and presentation.
What We Offer:
A dynamic work environment with opportunities for professional growth and development. Competitive compensation and benefits package. Collaborative team atmosphere.
-
Senior Clinical Trials Document Specialist
6 days ago
Belgaum, Karnataka, India beBeeResearch Full time ₹ 9,00,000 - ₹ 15,00,000Clinical Study ResearcherDelhi and Bangalore locations are open for this role.We seek a highly skilled Clinical Study Researcher to develop key clinical trial documents, including protocols, Investigator's Brochures (IBs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), and Clinical Study Reports (CSRs).The ideal candidate will be proficient in...
-
Careers in Clinical Trials
5 days ago
Belgaum, Karnataka, India beBeeClinicalResearch Full time ₹ 2,50,000 - ₹ 4,00,000We are seeking a detail-oriented professional to join our team in coordinating and executing clinical trials.Clinical Research Associate RoleThe ideal candidate will possess strong communication and organizational skills, with a eagerness to learn and grow in the clinical research domain.Key Responsibilities:Assist with on-site coordination of clinical trial...
-
Principal Biomedical Data Specialist
13 hours ago
Belgaum, Karnataka, India beBeeData Full time ₹ 1,50,00,000 - ₹ 2,50,00,000Job Summary:We are seeking a skilled Principal Biomedical Data Specialist to lead clinical data management activities across assigned clinical trials. This role will ensure high-quality data acquisition, database design, and data integrity.Lead clinical data management activities, overseeing the entire lifecycle of data from collection to reporting.Serve as...
-
Clinical Data Specialist
12 hours ago
Belgaum, Karnataka, India beBeeDataManagement Full time ₹ 5,00,000 - ₹ 10,00,000Job Title:Clinical Data SpecialistAbout the Role:We are seeking a highly skilled Clinical Data Specialist to take ownership of data management activities for our ongoing clinical studies.The ideal candidate will have end-to-end responsibility for data collection, cleaning, storage, quality control, and preparation of datasets for analysis, ensuring accuracy,...
-
Leading Statistician for Clinical Trials
5 days ago
Belgaum, Karnataka, India beBeeBiostatistician Full time ₹ 16,00,000 - ₹ 24,20,000Senior Biostatistician Job DescriptionThe Senior Biostatistician plays a pivotal role in leading and developing statistical strategies and deliverables to support clinical trials. Under the guidance of senior management, this position contributes to the planning, execution, and interpretation of statistical analyses across development programs.Key...
-
Clinical Data Validation Specialist
14 hours ago
Belgaum, Karnataka, India beBeeClinical Full time ₹ 18,00,000 - ₹ 24,00,000Job Title:Clinical Data Validation SpecialistKey Responsibilities:Utilize expertise in clinical data testing and validation to ensure data integrity.Collaborate with Clinical Data Scientists to develop effective testing strategies.Conduct user acceptance testing for clinical research forms, database edit checks, and exceptional reports/listings.Test clinical...
-
Senior Clinical Data Specialist
2 days ago
Belgaum, Karnataka, India beBeeDataAnalyzer Full time ₹ 12,00,000 - ₹ 16,00,000Develop and maintain data specifications, datasets and analysis for clinical trials.Create and validate tables, listings and figures for safety and efficacy parametersUnderstand and adhere to regulatory guidelines and operating proceduresEvaluate and ensure compliance with project specific requirementsSupport in developing ad hoc reports as neededEnsure...
-
Clinical Research Specialist
14 hours ago
Belgaum, Karnataka, India beBeeDermatology Full time ₹ 50,00,000 - ₹ 1,00,00,000Medical Dermatologist OpportunityWe are seeking a skilled Dermatologist to conduct clinical trials.Duties and Responsibilities:Conduct dermatological evaluations for diagnosing and treating various skin care conditions.Ensure adequate medical care is provided to subjects for adverse events, including significant laboratory values.Perform medical examinations...
-
Remote Clinical Systems Tester
5 days ago
Belgaum, Karnataka, India beBeeClinical Full time ₹ 10,00,000 - ₹ 14,00,000Job Summary:We are seeking a highly skilled Clinical Systems Tester with expertise in Veeva CDMS, eCOA, and IRT platforms to support testing and validation activities within a Decentralized Clinical Trial (DCT) environment.Key Responsibilities:Author and execute test scripts in Veeva EDC aligned with protocol requirements.Validate workflows across eCOA and...
-
Senior Clinical Data Analyst
13 hours ago
Belgaum, Karnataka, India beBeeLifeScience Full time ₹ 9,00,000 - ₹ 12,00,000PLSQL Developer for Life ScienceWe are seeking an experienced PLSQL developer with a strong background in life science to join our team.Key Responsibilities:Develop clinical trial reports using SAS, SQL and PLSQL as per study requirementsIdentify and raise protocol deviations in the databasePerform edit check validation by creating test cases and write test...