“From Staffing to Compliance—We’ve Got You Covered.”
At ClinNTech, you can find people from various Educational Institutes & Companies
Current Openings At ClinNTech
Safety Consultant
ClinNTech Consultants
Remote
6–12 Months (extendable)
Looking for an experienced Safety Consultant to manage adverse event reporting, safety data, and global compliance for clinical trials and devices.
Work Experience
- Bachelor’s in Life Sciences
- 3+ years in Pharmacovigilance
Skills
Regulatory CMC Manager
ClinNTech Consultants
Remote
Seeking an experienced Regulatory CMC Manager to lead global CMC regulatory strategies across development and commercial products. The role involves preparing and managing highquality CMC submissions, ensuring compliance with international requirements, and collaborating with cross-functional teams to support product lifecycle management.
Work Experience
- Bachelor’s/Master’s/Ph.D. in Chemistry, Pharmacy, Biochemistry, Chemical Engineering, or related field
- 5+ years in CMC Regulatory Affairs within pharma/biotech
- Proven experience with global submissions & regulatory agency interactions
Skills
Bioinformatician / Computational Biologist
ClinNTech Consultants
Remote (Limited Travel to Client Office)
6-Month Contract
We are seeking a Bioinformatician/Computational Biologist to support the integration and analysis of multi-omics datasets, with a focus on transcriptomics and genetics. The role involves data curation, QC, workflow development, and collaboration with research scientists on immunological disease studies.
Work Experience
- Master’s with 1+ years OR Bachelor’s with 3+ years in Bioinformatics, Computer Science, Statistics, or related field
- Hands-on experience in NGS data analysis, multi-omic workflows, and HPC/cloud systems
- Strong background in immunology-related research preferred
Skills
QC Analytical Chemist
ClinNTech Consultants
Research Triangle Park, NC
6–12 Months Contract
We are looking for a QC Analytical Chemist to perform analytical testing of raw materials, intermediates, and finished products while ensuring strict compliance with cGMP and regulatory standards. The role includes method development support, data review, instrument maintenance, and collaboration with QA, R&D, and production teams to maintain product quality.
Work Experience
- Bachelor’s or Master’s in Chemistry/Pharmaceutical Sciences
- 1–3+ years of QC lab experience in a GMP-regulated pharma/biotech environment
- Hands-on expertise with HPLC, GC, and UV-Vis required
Skills
Pharmacovigilance (PV) Manager
ClinNTech Consultants
Remote (Limited Travel to Client Office)
6–12 Months
We are seeking an experienced Pharmacovigilance Manager to lead PV operations, including case processing, signal detection, risk management, and regulatory safety reporting. The role requires deep knowledge of global PV regulations, oversight of safety databases and vendors, and cross-functional leadership to ensure patient safety and compliance throughout the product lifecycle.
Work Experience
- Bachelor’s/Master’s/PharmD/MD in Life Sciences, Pharmacy, or related field
- 5–8 years in Pharmacovigilance/Drug Safety within pharma, biotech, or CROs
- Hands-on experience with global PV operations, safety systems, and regulatory inspections
Skills
Your Next Career Move Starts Here
Submit your application and let’s build the future of healthcare together.
