Join Maiora and Advance Your Career in Clinical Research!
Summary:
Maiora is a dynamic and growing organization seeking talented and motivated individuals to join our team. We are currently hiring for three key positions: Lead Data Manager (Remote), Clinical Programmer (Remote), and Operational Specialist – Pharmacovigilance (Bangalore/Thane). These roles offer excellent opportunities for professional development, exposure to cutting-edge technologies, and the chance to contribute to impactful clinical research projects. If you are passionate about making a difference in healthcare and possess the required skills and experience, we encourage you to apply!
1. Lead Data Manager (Remote)
- Experience: 6+ Years
- Openings: 3
- Location: Remote
Job Overview:
Maiora is seeking an experienced and highly skilled Lead Data Manager to oversee end-to-end clinical data management (CDM) activities utilizing Veeva. As a Lead Data Manager, you will play a pivotal role in ensuring the quality, integrity, and accuracy of clinical data throughout the study lifecycle. This is an excellent opportunity for a proactive and detail-oriented individual with strong leadership abilities and a proven track record in CDM. Experience in study leadership and coding is a significant advantage.
Key Responsibilities:
- Lead and manage full-cycle Data Management activities, including study setup, conduct, and close-out.
- Oversee CRF design, data validation processes, and database management within the Veeva platform.
- Act as a primary point of contact for cross-functional communication with clinical teams, ensuring seamless collaboration.
- Review and effectively troubleshoot data queries, ensuring timely resolution and data integrity.
- Provide technical oversight on CDM standards, quality control measures, and adherence to project timelines.
Required Qualifications:
- A minimum of 6 years of hands-on experience in clinical data management.
- Demonstrated strong hands-on experience with the Veeva platform for CDM.
- 2-3 years of experience in a study leadership role, demonstrating the ability to guide and mentor teams.
- Coding knowledge is preferred.
- Excellent communication (both written and verbal) and documentation skills.
2. Clinical Programmer (Remote)
- Experience: 3–6 Years
- Openings: 4
- Location: Remote
Job Overview:
Maiora is looking for a skilled and detail-oriented Clinical Programmer to contribute to the design, development, and implementation of clinical trial databases and systems. The ideal candidate will have proven experience in Veeva forms design, edit checks, TSDV setup, coding configuration, and system migrations. As a Clinical Programmer, you will play a vital role in ensuring the efficient and accurate collection, management, and analysis of clinical trial data.
Key Responsibilities:
- Build and customize forms and dynamics within the Veeva platform.
- Develop and validate edit checks/rules to ensure data quality and consistency.
- Support TSDV, coding setup, and implement post-production changes as needed.
- Manage CRF updates, versioning, and system migrations, ensuring data integrity throughout the process.
- Collaborate effectively with Data Management and Clinical teams to ensure seamless integration and alignment of data management activities.
Required Qualifications:
- 3–6 years of experience in clinical programming.
- Strong working knowledge of Veeva programming workflows.
- Proven experience in study build, implementing data validation rules, and operational setup within clinical databases.
- Ability to troubleshoot and optimize EDC processes to improve efficiency and data quality.
3. Operational Specialist – Pharmacovigilance
- Experience: 1.5+ Years
- Location: Bangalore / Thane
Job Overview:
Maiora is seeking diligent and detail-oriented Operational Specialists to join our Pharmacovigilance team. As an Operational Specialist, you will be responsible for ICSR case processing and regulatory submission activities, ensuring compliance with global PV regulations and internal SOPs.
Key Responsibilities:
- Process Individual Case Safety Reports (ICSRs) in safety databases accurately and efficiently.
- Perform regulatory submissions in accordance with Standard Operating Procedures (SOPs) and relevant guidelines.
- Track and review incoming Adverse Event (AE) and endpoint information, ensuring timely and accurate data entry.
- Update case status, enter data, and perform coding using MedDRA terminology.
- Write clear and concise safety narratives and support literature monitoring activities.
Required Qualifications:
- 1.5+ years of experience in pharmacovigilance.
- Strong knowledge of global pharmacovigilance (PV) regulations and guidelines.
- Experience in ICSR processing, MedDRA coding, and narrative writing.
- Excellent analytical and documentation skills.
Why Join Maiora?
- Work on impactful global clinical research projects.
- Opportunity to work remotely (for select roles).
- Exposure to advanced Veeva-based workflows and technologies.
- Competitive salary package and benefits.
- Professional development and internal growth opportunities.
- Collaborative and supportive work environment.
How to Apply:
If you are a qualified and motivated candidate, we encourage you to apply! Please send your resume to [email protected].
Subject Line: Application – [Role Name]