Join us in advancing clinical research and making a meaningful impact in global healthcare.
At CLINEXEL we are always looking for talented and passionate professionals to join our growing team. We regularly post job opportunities across various functions on our LinkedIn, Facebook, Instagram pages. Follow us to stay updated on the latest openings and career opportunities:
Open Poistions
Clinical Research Associates (CRAs)
We are looking for Clinical Research Associates to support the successful execution of clinical trials through site monitoring and management activities.
Key Responsibilities:
– Conduct site qualification, initiation, monitoring, and close-out visits.
– Ensure compliance with protocol, GCP, and regulatory requirements.
– Review clinical data and maintain trial documentation.
– Liaise with investigators, site staff, and project teams.
Qualifications:
– Degree in Life Sciences, Pharmacy, Nursing, or related field.
– Knowledge of ICH-GCP guidelines and clinical trial processes.
– Prior monitoring experience preferred.
Open Poistions
Biostatistician
We are seeking experienced Biostatisticians to contribute to study design, statistical analyses, and interpretation of clinical trial data.
Key Responsibilities:
– Develop Statistical Analysis Plans (SAPs).
– Perform statistical analyses and generate study outputs.
– Collaborate with datan management and clinical teams.
– Support regulatory submissions and scientific publications.
Qualifications:
– Master’s degree or higher in Statistics, Biostatistics, Mathematics, or related discipline.
– Proficiency in SAS, R, or other statistical software.
– Experience in clinical research preferred.
Open Poistions
Pharmacovigilance Associate
Join our Pharmacovigilance team to support drug safety and risk management activities across clinical and post-marketing programs.
Key Responsibilities:
– Process and review adverse event reports.
– Perform case assessment, coding, and narrative writing.
– Ensure compliance with global pharmacovigilance regulations and timelines.
– Support signal detection and aggregate safety reporting activities.
Qualifications:
– Degree in Pharmacy, Medicine, Life Sciences, or related field.
– Knowledge of pharmacovigilance regulations and drug safety processes.
– Prior pharmacovigilance experience preferred.
Open Poistions
Medical Writer
We seek skilled Medical Writers to develop high quality clinical, regulatory, and publication documents. The candidate should possess strong scientific writing abilities.
Key Responsibilities:
– Prepare clinical study protocols, reports, informed consent forms, and regulatory documents.
– Develop manuscripts, abstracts, posters, and scientific publications.
– Ensure compliance with applicable regulatory and publication guidelines.
– Collaborate with cross functional teams to deliver high-quality documents within timelines.
Qualifications:
– Phd/MD, MBBS/BDS/BHMS/ BAMS, PharmD, MPharm, MSc Life Sciences, or equivalent.
– Experience in medical writing within the pharmaceutical, biotech, CRO, or healthcare industry preferred.
If you are interested in exploring a career with us, we encourage you to share your resume at careers@clinexel-cro.com. Our team reviews applications on an ongoing basis and will reach out when a suitable opportunity matches your profile.