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Position Summary:
We are seeking a highly organized, 20 hour per week Contractor to support the Non-Clinical Development team in managing regulatory documentation (CTA/IND) and coordination of Contract Research Organization (CRO) activities. This is ideal for candidates with one to three years experience in regulatory operations, non-clinical development, or CRO/vendor support within the biotech or pharmaceutical industry.
This role is critical to ensuring that documentation is submission-ready, timelines are met, and external partners are well-coordinated as we advance key programs toward clinical development.
The ideal candidate will be onsite one day per week.
Key Responsibilities:
Qualifications:
City Therapeutics is accepting resumes/CVs from direct applicants only. Recruitment Agency submissions will not be accepted at this time.
City Therapeutics is an Equal Opportunity and Affirmative Action employer committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
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