Clinical Data Manager (India, Hybrid/Remote) Data Management INDIA

MMS Holdings Inc; India; À distance; INR 600 000 - 1 000 000; Plein temps

Résumé du poste

MMS Holdings Inc. is a data-focused CRO offering global clinical research services. The role focuses on clinical data management and support for regulatory submissions.

As part of a collaborative team, you will contribute to eCRF development, data validation, query management, and UAT for EDC systems. A strong attention to detail and experience in CROs or pharma is essential.

Qualifications

• Bachelor’s Degree in a scientific, medical, or clinical discipline; Master’s or PhD preferred.
• 2-6 years of clinical data management experience.
• Hands-on experience with clinical trials and pharmaceutical development.
• Effective problem-solving and data analysis skills.
• Experience in the pharmaceutical or CRO industry.
• Experience with query and discrepancy management.
• Has a strong attention to detail.

Responsabilités

• Contribute to developing eCRFs, CRF Completion Guidelines, Edit check specs, and DMP.
• Contribute to study tracking and metric reports for use by the study team.
• Contribute to CRF tracking and data entry, integration of external electronic data, data validation and review, query processing and resolution, adverse event and medication coding, SAE reconciliation, database lock and database QC audits.
• Contribute to user acceptance testing (UAT) of EDC and integrated systems including executing of test plan and scripts.
• Assist with preparation for training sites/users training on EDC applications, and UAT.
• End user knowledge for study conduct activities including queries management, standard reporting and extracting data.
• Learning to develop data entry screens, dynamics, edit checks and other EDC components.

Connaissances

Data management

Analytical skills

Attention to detail

Problem solving

Formation

Bachelor’s degree in a scientific/medical/clinical discipline

Outils

EDC systems

Description du poste

Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team?MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.

Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit www.mmsholdings.comor follow MMS on LinkedIn.

Job Responsibilities

• Contribute to developing eCRFs, CRF Completion Guidelines, Edit check specs, and DMP.
• Contribute to study tracking and metric reports for use by the study team
• Contribute to CRF tracking and data entry, integration of external electronic data, data validation and review, query processing and resolution, adverse event and medication coding, SAE reconciliation, database lock and database QC audits.
• Contribute to user acceptance testing (UAT) of EDC and integrated systems including executing of test plan and scripts.
• Assist with preparation for training sites/users training on EDC applications, and UAT.
• End user knowledge for study conduct activities including queries management, standard reporting and extracting data.
• Learning to develop data entry screens, dynamics, edit checks and other EDC components.

Job Requirements

• Bachelor’s Degree in a scientific, medical, or clinical discipline or related field is required; Master’s or PhD preferred
• 2-6 years of previous experience in clinical data management
• Hands-on experience with clinical trials and pharmaceutical development preferred
• Effective problem-solving and data analysis skills
• Experience in the pharmaceutical or CRO industry must
• Experience with query and discrepancy management required
• Has a strong attention to detail