Clinical Data Manager III
3 weeks ago
At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.
We are looking for Clinical Data Manager III (CDM III) to join our A-team (hybrid*). As CDM III at Allucent, you will manage and coordinate DM deliverables from database design & set-up, through cleaning and reporting to database locking, ensuring that the completeness, accuracy and consistency of clinical data meets the quality standards and regulatory requirements for analysis and reporting.
In this role your key tasks will include:
Lead and serve as primary contact for DM with all relevant parties both internally ( Clinical Programmers, Data Scientists, Project Management, Clinical Operations/Monitoring, Clinical Monitoring, Biostatistics and other functional groups) and externally ( sponsors, vendors (EDC, external data), and investigational sites) Plan and project the resources required including management of tasks, timelines, risk and quality Monitor tasks against and keep track on budget, forecasts, identify and trigger changes of scope requests Develop, review and maintain project-specific DM documents including data management plan (DMP), eCRF specifications, data validation plan (DVP) and external data transfer agreements Lead and coordinate the development of clinical study database set-up, including eCRF design and database validation requirements Participate in the review of study documents ( protocol, Project Plan, safety plans/manuals and statistical analysis plan), lead and coordinate the review of (electronic) case report forms (eCRFs) Coordinate, participate and complete the database User Acceptance Testing (UAT) related tasks Create training materials for EDC users and provide project-specific training as required Review and validate clinical data to ensure consistency, accuracy, integrity and completeness Create data cleaning strategy in consultation with applicable functional groups and oversee data releases (such as for DETC/DSMB/IDMC, interim and final locks, updates after lock) Perform and/or coordinate various data transfers and reconciliation activities including (but not limited to) SAE, PK, and (other) external laboratory data Create and review project metric reports, status updates, study progress to Lead DM in order to share information on site performance issues, data trends and protocol non-compliance Support and conduct Quality Review checks during study. As lead DM, may organize and lead Quality Review activities Assist in contracts negotiation and contracting process with vendors (EDC, IRT, eCOA) Manage the database maintenance, lock and close-out processes and procedure Participate in conference calls and/or meetings with vendors and sponsors Recognize and solve potential problems and evaluate effectiveness Maintain DM study documentation on an ongoing basis and ensure that all filing is up to date Plan and create necessary documentation to support internal and external audits; may participate in such audits assigned Help to align data management and clinical programming best practices, standards and conventions within the company Propose and support initiatives for improving efficiencyRequirements
To be successful you will possess:
Minimum Educational Requirement: Preferably Life science graduate or equivalent qualification 5+ years’ experience in clinical data management experience within Contract Research Organization (CRO), Pharmaceutical or biotech industries Proven knowledge of clinical data management process and clinical database systems, including Electronic Data Capture applications. Good communication skills written and verbal. Effective working knowledge of Microsoft Office Suite including Word and Excel. Demonstrated proactiveness, problem solving, analytical, organizational and time management skills. Demonstrated flexibility and ability to work well in a fast faced growing organization. Demonstrated ability to work in a global team environment. Demonstrates basic understanding of Clinical Trials and the flow of data. Demonstrated ability to be compliant with ICH-GCP/regional regulatory guidelines and POI SOPs. Comprehension of study documentation standards including Trial Master File organization and archival processes. Familiarization of data standards, preferably CDISC STDM.Benefits
Benefits of working at Allucent include:
Comprehensive benefits package per location Competitive salaries per location Departmental Study/Training Budget for furthering professional development Flexible Working hours (within reason) Opportunity for remote/hybrid* working depending on location Leadership and mentoring opportunities Participation in our enriching Buddy Program as a new or existing employee Internal growth opportunities and career progression Financially rewarding internal employee referral program Access to online soft-skills and technical training via GoodHabitz and internal platforms Eligibility for our Spot Bonus Award Program in recognition of going above and beyond on projects Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employeesDisclaimers:
*Our hybrid work policy encourages a dynamic work environment, prescribing 2 days in office per week for employees within reasonable distance from one of our .
“The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively “Allucent”). Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third-party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources.”
-
Clinical Data Manager III
3 weeks ago
bangalore, India Allucent Full timeAt Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. We are looking for Clinical Data Manager III (CDM III) to join our A-team (hybrid*). As CDM III at Allucent, you will manage and coordinate DM...
-
Clinical Data Manager
4 weeks ago
bangalore, India George Clinical Full timeWe 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 excellence20+ years of...
-
Clinical Data Manager
4 weeks ago
bangalore, India George Clinical Full timeWe 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...
-
Associate Clinical Data Manager
4 weeks ago
bangalore, India BAN Fortrea Clinical Development Pvt Ltd Full timeAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...
-
Associate Clinical Data Manager
4 weeks ago
Bangalore, India BAN Fortrea Clinical Development Pvt Ltd Full timeAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...
-
Director - Clinical Data Management
4 weeks ago
Bangalore, India AstraZeneca Full timeJob Title: Director - Clinical Data Management Career Level - F Introduction to role: Join us at AstraZeneca as a Director of Clinical Data Management, where you 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. You will be a key...
-
Director - Clinical Data Management
4 weeks ago
bangalore, India AstraZeneca Full timeJob Title: Director - Clinical Data Management Career Level - F Introduction to role: Join us at AstraZeneca as a Director of Clinical Data Management, where you 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. You will be...
-
Senior Clinical Database Developer
4 weeks ago
bangalore, India George Clinical Full timeWe 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...
-
Clinical Research Coordinator
3 weeks ago
bangalore, India MS CLINICAL RESEARCH Full timeJob Title : Clinical Research Coordinator Company : MS Clinical Research Pvt Ltd About Us : MS Clinical Research (MSCR) is a dynamic and forward-thinking clinical research organization dedicated to conducting cutting-edge clinical trials. We are committed to advancing medical science and contributing to the development of innovative healthcare solutions. Job...
-
bangalore, India MS CLINICAL RESEARCH Full timeJob Title : Business Development Manager-Clinical Services and PharmaLocation : BengaluruCompany : MS Clinical Research Pvt LtdAbout Us:MS Clinical Research Pvt Ltd is a leading organization in the clinical research industry, providing comprehensive clinical services to the pharmaceutical sector. We are committed to advancing scientific knowledge and...
-
Clinical Trial Data Manager
4 weeks ago
bangalore, India Novo Nordisk AS Full timeDepartment: Data Management & Centralised Data Review Are you ready to take on a challenging Clinical Trial Data Manager role? Do you have experience in clinical trial data management and a passion for ensuring high-quality data delivery? Join our Trial Data Management team in Bangalore, India, and make a difference in the healthcare field. Read on...
-
Clinical Study Quotation Specialist
3 weeks ago
bangalore, India MS CLINICAL RESEARCH Full timeCompany Description: MS Clinical Research is a dynamic and innovative organization dedicated to advancing healthcare through clinical research. We are committed to excellence in every project, ensuring that our clients receive the most accurate and competitive quotes for their clinical studies. Job Summary: We are seeking a detail-oriented and analytical...
-
Clinical Data Management Intern
2 weeks ago
bangalore, India Pride Circle Full timeHiring LGBT Apprentices/Interns only Role: Clinical Data Management Specialist - Intern Company:Big Pharma Company - 80% would refer their friends) Experience: Freshers only Work Location: Bangalore Employment: Full-time Who Can Apply: LGBT candidates as this is a Diversity hiring initiative. Please send CVs if you are from the LGBT Community ONLY at We...
-
Clinical Data Management Trainer
2 weeks ago
bangalore, India Learning Lab Full timeCompany DescriptionWe offer training and placement support for courses like Data Science, Analytics, Cloud, Cyber, and Digital Marketing.Role DescriptionThis is a full-time on-site role as a Clinical Data Management Trainer along with Medical Writing and Regulatory Affair located in Bengaluru. As a Clinical Data Management Trainer, you will be responsible...
-
Clinical Trial Data Manager
4 weeks ago
bangalore, India Novo Nordisk Full timeDepartment : Data Management & Centralised Data Review Are you ready to take on a challenging Clinical Trial Data Manager role? Do you have experience in clinical trial data management and a passion for ensuring high-quality data delivery? Join our Data Management & Centralized Data Review team in Bangalore, India, and make a difference in the...
-
Senior Clinical Trial Data Manager
4 weeks ago
bangalore, India Novo Nordisk AS Full timeDepartment: Data Management & Centralised Data Review Are you ready to take on a challenging Senior Clinical Trial Data Manager role? Do you have experience in clinical trial data management and a passion for ensuring high-quality data delivery? Join our Data Management & Centralised Data Review team in Bangalore, India, and make a difference in the...
-
Senior Clinical Trial Data Manager
4 weeks ago
bangalore, India Novo Nordisk Full timeDepartment: Data Management & Centralised Data Review Are you ready to take on a challenging Senior Clinical Trial Data Manager role? Do you have experience in clinical trial data management and a passion for ensuring high-quality data delivery? Join our Data Management & Centralised Data Review team in Bangalore, India, and make a difference in...
-
Senior Clinical Data Manager II
3 weeks ago
bangalore, India AstraZeneca Full timeJob Title - Senior Clinical Data Manager II Career Level - D Introduction to role: Join us as a Senior Clinical Data Manager II in our Oncology R&D department. In this role, you will be responsible for the coordination of the Clinical Data Management (CDM) deliverables on assigned clinical studies. You will act as a core member of the Global...
-
Senior Clinical Data Manager
4 weeks ago
bangalore, India MUM Fortrea Development India Pvt Ltd Full timeAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...
-
Senior Clinical Data Manager
4 weeks ago
Bangalore, India MUM Fortrea Development India Pvt Ltd Full timeAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...
