Xogene Services LLC, a reputable name in the clinical data transparency industry, is dedicated to supporting pharmaceutical and healthcare companies in meeting regulatory requirements for clinical trial transparency. Operating with a global mindset, Xogene offers comprehensive solutions for managing, anonymizing, and submitting clinical trial data to regulatory platforms like Clinicaltrials.gov and EudraCT. With a focus on collaboration, precision, and regulatory compliance, Xogene provides essential services that ensure the responsible disclosure of clinical trial data.

Role Overview: Clinical Trials Transparency Junior Analyst

Xogene is inviting applications for the role of Clinical Trials Transparency Junior Analyst (CTTJA) at their Pune location. This entry-level position is ideal for candidates who are currently pursuing a Bachelor’s degree in Pharmacy and are expected to graduate by 2025, with the intended start date being July 2025. The CTTJA will play a pivotal role in handling clinical trial data, particularly by ensuring accurate data entry and document redactions. This position offers an excellent opportunity to gain hands-on experience in clinical trial transparency and regulatory compliance.

Key Responsibilities

As a Clinical Trials Transparency Junior Analyst, you’ll be involved in a wide range of tasks essential for the effective operation of Xogene’s transparency projects:

• Data Redaction and Entry: Enter clinical trial data from source documents directly into regulatory databases, ensuring accuracy and confidentiality.
• Peer Review and Quality Control: Perform quality checks on redacted documents to confirm accuracy and completeness.
• Document Anonymization: Assist in the redaction of sensitive data from clinical trial documents, helping to maintain patient privacy and confidentiality.
• Project Coordination: Regularly communicate with team members to meet project deadlines and proactively manage deliverable timelines.
• Team Collaboration: Work closely with the Clinical Trials Transparency (CTT) team to ensure high standards of data accuracy and regulatory compliance are met.

Qualifications and Skills Required

To excel in this role, candidates must meet the following requirements:

1. Educational Background: Bachelor’s degree in Science or a related field (Pharmacy students graduating in 2025 are preferred).
2. Interest in Life Sciences: A strong enthusiasm for life sciences and a desire to learn about clinical trial transparency and regulatory processes.
3. Attention to Detail: A meticulous eye for detail is critical, given the role’s data-sensitive and compliance-focused nature.
4. Communication Skills: Excellent written and verbal communication abilities, with proficiency in Microsoft Office (Excel, PowerPoint, Word).
5. Intercultural Understanding: Ability to collaborate in a global, multicultural environment, with a keen sense of teamwork and a proactive attitude.

Application Link (first Open Microsoft Account)