Clinical Data Coordinator Ii
2 weeks ago
As a Clinical Data Coordinator-II you will be actioning all tasks relating to Clinical Data Management from the start to the finish of a study and to support Project Manager in studies across DM functions.
Quanticate is the world leading data-focused CRO, and we often work with our customers on their complicated clinical trials which require a high level of statistical programming, statistics and data management input. We need talented individuals to help us fulfil our customers’ needs.
Our customers range from top global pharmaceutical companies where you can work as an integrated team member on a world leading clinical program, to small biotechs that are taking their first steps in clinical development
We strongly advocate career development providing membership to professional societies, encouraging your involvement in their activities and committees. Together we can help you build the career you want - developing your skills, working on challenging problems, to ultimately develop clinical therapies that matter.
**Responsibilities**
- To assist in the testing of databases prior to activation.
- To assist in the preparation of study specific documentation as appropriate.
- To critically review CRFs as specified in the Data Management Plan and to query any errors or omissions with either the study sponsor or the investigator as required.
- To track and resolve Data Clarification Forms in the study specific Database.
- To resolve Self-Evident Queries/Allowable Changes in the study specific Database.
- To perform the Quality Control of Data Entry and CRF/database as appropriate.
- To prepare any documentation for return to client/internal archiving at study completion as requested.
**Requirements**:
- Extensive knowledge of at least 2 Clinical Data Management systems such as Oracle Clinical, Medidata Rave, Inform.
- Extensive experience in Clinical data management activities from the start to the finish of a study
- Thorough knowledge of ICH Guidelines and GCP including regulatory requirements for the conduct of clinical development programs, especially as related to data handling and processing.
**Benefits**
Competitive Salary (Open to discussion based on experience)
Flexible working hours
18 days Annual leave plus casual, sick leave
Medical Insurance
Accidental Coverage
5, 10, 15 years of service recognition awards
Death in service scheme - 3x base salary
Long Term Disability Insurance
Quanticate offers a variety of different learning development opportunities to help you progress (mentoring, coaching, e-learning, job shadowing)
-
Clinical Research Coordinator
1 week ago
Domlur, Bengaluru, Karnataka, India MS CLINICAL Full time**Job Title**: Clinical Research Coordinator (minimum 1 year of experience)** **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...
-
Clinical Data Associate Ii
8 hours ago
Bengaluru, India Novotech Asia Full timeBrief Position Description: Supports the day-to-day operations of the data management projects, providing in-house data entry support to projects and administrative support to CDMs, according to GCDMP guidelines, local regulatory requirements, and Novotech/Client SOPs. Minimum Qualifications & Experience: Graduate in a clinical or life sciences related...
-
Clinical Data Associate Ii
2 days ago
Bengaluru, Karnataka, India Precision for Medicine Full time**Position Summary**: The Clinical Data Associate II provides data management support and assistance in all aspects of the clinical trial data management process from study start up to post database lock for assigned projects under direct supervision. Standard Operating Procedures / Work Instructions (SOPs/WIs); regulatory directives; study specific plans...
-
Clinical Data Associate Ii
8 hours ago
Bengaluru, India Novotech Asia Full time**Organization Description** Novotech is a leading Asia-Pacific biotech specialist CRO and consists of two operating brands, Novotech and PPC. Novotech is a clinical CRO with labs, phase I facilities, and drug development consulting services. It has accumulated experience in over 3,700 clinical projects, including Phase I to Phase IV clinical trials and...
-
Clinical Data Associate Ii
2 days ago
Bengaluru, Karnataka, India Precision Medicine Group Full timeBangalore Karnataka India; Chennai **Job Type**: Regular Full-time Division: Precision for Medicine Business Unit: Clinical Solutions Requisition Number: 5545 **Position Summary**: The Clinical Data Associate II provides data management support and assistance in all aspects of the clinical trial data management process from study start up to post database...
-
Clinical Data Manager 1
2 days ago
Bengaluru, Karnataka, India Emerald Clinical Full time ₹ 9,00,000 - ₹ 12,00,000 per yearAt Emerald Clinical, we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region. We are dedicated to advancing clinical research through scientific expertise and operational excellence, supporting biopharmaceutical, medical device, and diagnostic customers across all trial phases, from registration to...
-
Clinical Research Associate
4 weeks ago
Bengaluru, India MS CLINICAL RESEARCH Full timeJob Title : Clinical Research Associate (CRA)Company : MS Clinical Research Pvt LtdExperience : Minimum 3 yearsAbout Us :MS Clinical Research (MSCR) is a leading clinical research organization dedicated to advancing scientific discovery and improving healthcare outcomes. We are committed to conducting high-quality clinical trials and contributing to the...
-
Clinical Data Coordinator
2 days ago
Bengaluru, Chennai, Hyderabad, India Airvin Skills Full time ₹ 4,00,000 - ₹ 6,00,000 per yearThe Clinical Data Coordinator (Intern/Fresher Level) plays a crucial role in ensuring the integrity and quality of clinical trial data. This position offers a valuable entry point into the field, providing hands-on experience in core data management tasks and industry best practices.Key Responsibilities:Data Entry and Verification:Meticulous data entry into...
-
Clinical Research Associate
4 weeks ago
Bengaluru, India MS CLINICAL RESEARCH Full timeJob Title: Clinical Research Associate (CRA)Company: MS Clinical Research Pvt LtdExperience: Minimum 3 yearsAbout Us:MS Clinical Research (MSCR) is a leading clinical research organization dedicated to advancing scientific discovery and improving healthcare outcomes. We are committed to conducting high-quality clinical trials and contributing to the...
-
Clinical Research Associate
3 weeks ago
Bengaluru, India MS CLINICAL RESEARCH Full timeJob Title : Clinical Research Associate (CRA) Company : MS Clinical Research Pvt Ltd Experience : Minimum 3 years About Us : MS Clinical Research (MSCR) is a leading clinical research organization dedicated to advancing scientific discovery and improving healthcare outcomes. We are committed to conducting high-quality clinical trials and contributing to the...