The Clinical Associate Graduate is an entry-level role frecent graduates entering the clinical research industry through Novotech’s structured Graduate Program. The role combines formal training with supervised, on-the-job experience to build foundational skills in clinical trial conduct, site management, regulatory compliance. The position supports Clinical Research Associate (CRA) activities under close supervision, with a defined pathway toward progression to CRA I subject to performance readiness.
Job Responsibilities:
• Participate fully in the Graduate Training Program, including structured learning, functional rotations assessments.
• Demonstrate commitment to continuous learning by participating in coaching mentoring activities with Line Managers, cross functional stakeholders, the assigned SeniCRA, graduate cohort peers.
• Support CRAs with supervised site management activities, including maintenance of essential site documentation InvestigatSite Files.
• Assist with Trial Master File (TMF) coordination, document filing, quality checks ongoing completeness.
• Support preparation fmonitoring visits, participation in co‑monitoring observational visits, completion of routine follow‑up activities under guidance.
• Support data review, query resolution maintenance of clinical trial systems (e.g. CTMS, eTMF, eCRF) under supervision.
• Provide in‑house support to clinical trial teams on assigned studies, including communication with internal teams, sites vendors to request documentation, resolve routine queries perform elements of in‑house CRA activities, subject to training completion demonstrated capability.
• Assist with general study administration activities, including basic finance, regulatory, safety study close‑out support under supervision.
• Apply Novotech quality standards, ICH GCP regulatory requirements in all activities, escalating risks, issues safety concerns promptly to the supervising CRA Line Manager.
• Be aware of adhere to company processes relevant to clinical trial delivery, demonstrate a quality‑focused approach to work, assist in the review development of clinical SOPs processes as appropriate.
• UnderstNovotech’s responsibilities as a service provider within the pharmaceutical biotech industry ensure all internal external communications reflect a professional company image.
Minimum Qualifications & Experience:
• Recent graduate in a clinical life sciences-related field.
• Strong learning agility, attention to detail,ganisational time management skills, with the ability to work effectively in a team use computer-based systems confidently.
• Ability willingness to travel in the role post-programme.
Novotech is proud to offer a great workplace.We are committed to being an employer of choice fgender equality providing an inclusive work environment where everyone is treated fairly with respect.
Our team members are passionate about what we do,but we understwork is only one of the things that is important to them.We support our team members with flexible working options,paid parental leave fboth parents,flexible leave entitiements,wellness programs ongoing development programs.
We are looking fpeople who are passionate about working clinical research andbiotech,including people who identify as LGBTIQ+,have a disability have caring responsibilities.
We are a Circle Back Initiative Employer commit to respond to everypplication.We look forward to talking to you about working at Novotech.
接受26届应届毕业生投递
截止日期：2027年04月27日
招聘人数：1人
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