CURRENT OPENINGS
Biostatistician (0–3 Years)
We're Hiring: Biostatistician (0–3 Years)
Location: Remote, India
Type: Full-time
Experience Level: Entry to Junior (0–3 years)
We are looking for a Biostatistician with hands-on experience in Pharmacokinetic (PK) analysis to support ongoing clinical studies.
Responsibilities:
> Perform non-compartmental PK analyses for interim and final reports.
> Conduct interim and final PK analyses.
> Prepare PK-related outputs for SRC meetings.
> Contribute to SAP and PK-specific mock shell.
> Assess PK populations and support SAP-driven deliverables.
> Review SDTM and ADaM datasets for PK analyses.
> Generate tables, listings, and figures.
> Review and QC PK TFLs and contribute to the CSR as needed.
> Evaluate PK data transfer agreements.
> Prepare and contribute to the final PK report.
Statistical Programmer I (1–3 Years Experience & 5+ Years Experience) | Remote (WFH)
We're actively hiring for two key roles to support growing global studies.
1. Statistical Programmer I (1–3 Years Experience) | Remote (WFH)
Responsibilities:
• Create annotated CRFs (aCRF) for SDTM mapping.
• Develop SDTM and ADaM specifications aligned with study protocols.
• Program and validate SDTM and ADaM datasets per CDISC standards.
• Generate Define.XML & Reviewer's Guides (SDRG/ADRG) for submissions.
• Create TLF outputs for clinical and statistical reporting.
• Support programming automation and best practices.
Education & Experience:
• Bachelor’s degree in life sciences, biostatistics, or similar.
• 1–3 years of SAS programming experience in a CRO/pharma setting.
• Solid knowledge of SDTM, ADaM, and TLF development.
• Exposure to R programming is an added advantage.
• Strong attention to detail with good documentation skills.
2. Senior Statistical Programmer (5+ Years Experience) | Remote (WFH)
Key Responsibilities:
• Lead statistical programming for assigned clinical studies.
• Guide creation of aCRFs and metadata mapping for SDTM.
• Develop & review SDTM and ADaM specifications.
• Program and QC CDISC-compliant SDTM/ADaM datasets.
• Generate and audit Define.XML and Reviewer's Guides (SDRG/ADRG).
• Oversee TLF creation and validation for clinical outputs.
• Mentor junior team members and drive technical excellence.
• Support programming process improvements and automation.
Essential Qualifications:
• Bachelor’s/Master’s in Statistics, Computer Science, or related fields.
• 5+ years of hands-on SAS programming experience in clinical trials.
• Proven experience leading complex studies.
• Strong knowledge of CDISC SDTM & ADaM, Define.XML, and regulatory expectations.
• SAS Macro and Graph expertise; R experience preferred.
Content Creator & Graphic Designer
We are looking for a Content Creator & Graphic Designer who can conceptualize, write, design, and deliver engaging content that reflects the Oryxion brand. The ideal candidate has strong storytelling skills, understands modern design, and can translate technical/clinical content into visually compelling narratives.
If you enjoy working end-to-end—from idea to execution—across social, digital, and corporate branding, this role is for you.
✨ Key Responsibilities
Branding & Visual Design
• Create high-quality designs for brochures, corporate decks, department presentations, flyers, posters, banners, and branding assets.
• Develop visuals for social media, LinkedIn, and marketing campaigns aligned with Oryxion’s brand identity.
• Enhance and maintain Oryxion’s visual identity, ensuring brand consistency across all platforms.
Digital Content Creation
• Write and design content for website pages, landing sections, case studies, blogs, product/service descriptions, and email campaigns.
• Conceptualize and produce engaging content for LinkedIn, Instagram, YouTube (if required) and short-form videos/reels.
• Convert complex clinical/technical information into easy-to-understand content and visuals.
Marketing & Campaign Support
• Create digital assets for paid ads, webinars, conferences, and promotional events.
• Support brand-building initiatives through compelling storytelling, infographics, and marketing collateral.
Cross-Functional Collaboration
• Work with leadership, marketing, HR, and technical teams to understand requirements and deliver creative solutions.
• Co-create content with writers, subject-matter experts, and project teams for internal and client-facing materials.
Creative Leadership
• Contribute ideas for improving brand communication, visual direction, and content strategy.
• Continuously explore new design trends, formats, and tools to elevate creative output.
📌 Requirements
• 2–5 years of experience in content creation + graphic design (preferably in corporate, B2B, tech, life sciences, or healthcare).
• Strong portfolio showcasing writing + design work (social media creatives, brochures, presentations, website content, etc.).
• Proficiency in Adobe Creative Suite (Illustrator, Photoshop, InDesign), Canva, Figma, or similar tools.
• Strong command over English communication (writing + storytelling).
• Ability to visualize technical/clinical concepts and convert them into engaging designs.
• Experience designing for social media, corporate presentations, and web content.
• Ability to manage multiple projects simultaneously and deliver within timelines.
• Knowledge of video editing or motion graphics is an added advantage.
Clinical Data Coordinator II (3-5 Years Experience)
Requirements
- Experience:
- Minimum of 3-5 years of experience in clinical data management or a related field.
- Experience with clinical trials and knowledge of Good Clinical Practice (GCP) CDISC-CDASH and regulatory requirements (e.g., FDA, EMA).
- Proficiency in using Electronic Data Capture (EDC) systems and clinical trial management software (e.g., Medidata, Oracle Clinical).
- Technical Skills:
- Strong knowledge of database management and data cleaning query management and reconciliation.
- Proficiency in statistical software (e.g., SAS, SPSS) and data visualization tools.
- Familiarity with coding languages such as SQL or Python is a plus.
- Analytical Skills:
- Ability to analyse and interpret clinical data.
- Strong problem-solving skills and attention to detail.
- Communication Skills:
- Excellent verbal and written communication skills.
- Ability to work collaboratively in a team environment and with cross-functional teams.
- Certification:
- Professional certification in clinical data management (e.g., CCDM from SCDM) is an advantage.
Senior Quality Assurance Associate (3-5 Years Experience)
Oryxion is seeking a detail-oriented and proactive Senior Quality Assurance Associate to strengthen our Quality Management System and ensure compliance across all clinical and data operations. This role plays a key part in maintaining quality oversight for our core service areas—Statistical Programming, Biostatistics, Clinical Data Management, Medical Writing, and Regulatory Affairs.
You will be responsible for supporting and monitoring QA processes, managing documentation, coordinating audits, and ensuring that Oryxion’s operations consistently align with international quality standards including GCP, ICH, ISO 9001:2015, and ISO 27001:2022.
The ideal candidate will bring both technical knowledge and a strong sense of ownership toward maintaining excellence in quality and compliance.
What You’ll Do
• Maintain and enhance Oryxion’s Quality Management System (QMS), ensuring all documentation, SOPs, and templates remain compliant and current.
• Coordinate internal, client, and vendor audits—from planning and preparation to follow-up and CAPA tracking.
• Oversee training compliance across teams and ensure timely completion and acknowledgment of required quality documents.
• Collaborate with IT, Data Management, and Programming teams on GxP system validation and CSV documentation.
• Review, organize, and archive controlled documents within electronic systems for traceability and audit readiness.
• Prepare QA metrics, management review inputs, and summary reports to highlight trends and improvement opportunities.
• Provide day-to-day support to operational teams on GCP, SOPs, and regulatory compliance requirements.
• Promote continuous improvement initiatives and contribute to maintaining a strong culture of quality within the organization.
Who You Are
• Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or a related field.
• 3–5 years of experience in QA within a CRO, pharmaceutical, or life-sciences environment.
• Strong understanding of GCP, ICH, GDPR, ISO, and general quality frameworks.
• Experience supporting or conducting audits and system validation activities.
• Excellent communication and collaboration skills, with the ability to engage across functions.
• Skilled in MS Office and electronic documentation systems, with high attention to detail.
• Self-motivated, analytical, and capable of handling multiple priorities with accountability.