Innovators Wanted

🚨 We Are Hiring: Clinical SAS Teaching Faculty Trainer 🚨

CareerInPharma is looking for a part-time experienced Clinical SAS Trainer to join our expert team and train the next generation of clinical programmers. If you have strong industry experience and a passion for mentoring, this is your chance to make a meaningful impact!

Key Responsibilities:
✅ Design and deliver structured training programs on Clinical SAS, with a focus on real-world applications in clinical trials and data management.
✅ Teach key SAS modules including BASE SAS, ADVANCED SAS, and SAS for clinical trials (CDISC: SDTM & ADaM).
✅ Guide learners through hands-on projects, case studies, and clinical data analysis exercises.
✅ Stay updated on industry tools, clinical trial standards, and regulatory data requirements (FDA, CDISC, ICH-GCP).
✅ Collaborate with internal teams to continuously improve training content and delivery methods.

Who Can Apply?
🎓 Qualification: Bachelor’s/Master’s in Life Sciences, Pharmacy, Statistics, Doctor degrees (MBBS, BDS, BHMS, BAMS, BUMS, etc), or a related field.
📌 Experience: 3 to 5 years of experience in Clinical SAS programming in CROs, pharma companies, or clinical research.
💡 Skills: Expertise in SAS programming, familiarity with CDISC standards (SDTM/ADaM), and excellent communication skills.

📩 Interested? Send your resume to the attached apply now link

🔹 Join CareerInPharma & inspire future clinical SAS professionals to excel in the pharmaceutical industry!

CareerInPharma is looking for an experienced Regulatory Affairs Trainer to join our team and contribute to the professional development of aspiring regulatory professionals. If you have hands-on industry experience and a passion for teaching, this could be the perfect opportunity for you!

Key Responsibilities:
✅ Develop and deliver comprehensive training programs on pharmaceutical regulatory affairs, ensuring alignment with the latest industry regulations.
✅ Provide expert guidance on regulatory documentation, submission processes, and compliance strategies.
✅ Stay updated on evolving regulatory guidelines (USFDA, EMA, CDSCO, ICH, etc.) and incorporate them into training modules.
✅ Collaborate with cross-functional teams to enhance learning outcomes.

Who Can Apply?
🎓 Qualification: M.Pharm or Healthcare professionals with relevant regulatory experience are also welcome!
📌 Experience: 3 to 5 years of core industry experience in regulatory affairs.
💡 Skills: In-depth knowledge of regulatory guidelines, excellent communication & presentation skills, ability to simplify complex regulatory information.