Senior Clinical Research Associate I Flex

Novotech; Philippines; On-site; PHP 600,000 - 900,000; Full time

Job summary

Novotech is seeking a Senior Clinical Research Associate I (Flex) in the Philippines to manage and monitor clinical projects in line with ICH-GCP, SOPs, and PMP requirements.

The role involves site qualification, monitoring visits, consent verification, audit readiness support, and potential mentorship of junior CRAs. Strong English and organizational skills are essential.

Qualifications

• A 4-year BS degree or equivalent experience. Advanced degree is a plus.
• At least 3 years of experience in a clinical research environment.
• Good command of written and spoken English or another second language.
• Good organization and communication skills.
• High attention to detail and accuracy.
• Demonstrated ability to attain and maintain a working knowledge of GCPs and applicable SOPs.

Responsibilities

• Contribute comments/input in the development of Protocol, Informed Consent Form (ICF), Case Report Forms (CRF) and other project related documents.
• Perform site qualification, site initiation, interim monitoring, site management and close-out visits (on-site or remotely) ensuring regulatory, ICH-GCP and/or GPP compliance.
• Verify the process of obtaining informed consent and protect confidentiality; assess factors affecting patient safety and data integrity.
• Prepare for and attend Investigator Meetings and sponsor meetings; may lead meetings and training sessions as applicable.
• Provide guidance toward audit readiness and support preparation for audits and follow-up actions.
• May provide training or mentorship to junior CRAs; may perform training and sign-off visits.
• May be mentored and assigned clinical operations lead tasks under supervision.

Education

Bachelor of Science degree

Job description

Senior Clinical Research Associate I Flex

Company: Novotech. Job Type: Full Time. Philippines.

Clinical Research Associate (CRA) Job Description

The Clinical Research Associate (CRA) is responsible for managing and monitoring the conduct of clinical projects according to ICH-GCP, Standard Operating Procedures (SOP), and applicable Project Management Plan (PMP) and local regulatory requirements.

Job Responsibilities

• Contribute comments/input in the development of Protocol, Informed Consent Form (ICF), Case Report Forms (CRF) and other project related documents.
• Perform site qualification, site initiation, interim monitoring, site management and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. Use judgment and experience to evaluate overall performance of site and site staff and provide recommendations regarding site‑specific actions; immediately communicate/escalate serious issues to the project team and develop action plans. Maintain a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes.
• Verify the process of obtaining informed consent has been adequately performed and documented for each subject/patient as required/appropriate. Demonstrate diligence in protecting the confidentiality of each subject/patient. Assess factors that might affect subject/patient's safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues.
• Prepare for and attend Investigator Meetings and/or sponsor face‑to‑face meetings. Participate, and may, with supervision, lead global clinical monitoring/project staff meetings (inclusive of Sponsor representation, as applicable) and attend clinical training sessions according to the project‑specific requirements.
• Provide guidance at the site and project level towards audit readiness standards and support preparation for audit and required follow‑up actions.
• May provide training or mentorship to more junior level CRAs. May perform training and sign‑off visits for junior CRA staff, as assigned.
• May be mentored and assigned clinical operations lead tasks under supervision of an experienced Clinical Operations Lead (COL), or operational line manager.
• As required, collaborate and build relationships with sponsor and other affiliates.

Qualifications

• A 4‑year BS (Bachelor of Science) degree or equivalent experience. Advanced degree is a plus.
• At least 3 years of experience in a clinical research environment.
• Good command of written and spoken English or another second language.
• Good organization and communication skills.
• High attention to detail and accuracy.
• Demonstrated ability to attain and maintain a working knowledge of GCPs and applicable SOPs.