Clinical study documentation jobs

Sr Staff Clinical Technical Program Manager, APAC

Dexcom · Posted Nov 6, 2026

Open

Sydney, New South Wales, Australia
Hybrid
Full-time · Senior
13+ years

Sr Staff Clinical Technical Program Manager, APAC

Dexcom · Posted Nov 6, 2026

Open

Sydney, New South Wales, Australia
Hybrid
Full-time · Senior
13+ years

Sr Staff Clinical Technical Program Manager, APAC

Dexcom · Posted Nov 6, 2026

Open

Sydney, New South Wales, Australia
Hybrid
Full-time · Senior
13+ years

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Lead planning and execution of complex clinical programs across the Asia Pacific region, driving multi‑country studies and collaborating with global stakeholders.

Responsibilities

Lead planning and execution of complex clinical programs across APAC
Provide strategic direction and leadership to clinical study teams
Partner with cross‑functional core teams and external CROs
Develop and implement clinical study strategies
Manage study operations, timelines, budgets, and performance metrics

Requirements

Bachelor’s degree in a technical discipline
Master’s degree with 8+ years equivalent industry experience
PhD with 5+ years experience
Nice to have: experience managing external CROs for Class II and Class III medical device studies
Nice to have: experience supporting diabetes or digital health studies

Skills

clinical research regulations Good Clinical Practice (GCP)medical device industry experience project management budget management

Inhouse Clinical Research Associate - SA

Novotech Global · Posted Nov 6, 2026

Open

Australia
12+ years

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Support the clinical team’s in‑house activities on assigned projects, manage documentation, coordinate trial materials, and assist with monitoring visits.

Responsibilities

Support the clinical team’s in‑house activities on assigned projects
Co‑ordinate and maintain clinical study documentation in the Trial Master Files (TMF)
Support the clinical team in essential document development, collection and management process
Manage the Clinical Trial Management System (CTMS)
Create the Investigator Site Files, co‑ordinating the ordering, dispatch and tracking of trial materials

Skills

ICH GCP guidelines Good Documentation Practice Clinical Trial Management System (CTMS)Trial Master Files (TMF)Clinical study documentation Audit preparation QC reviews

See full job description

Sr Staff Clinical Technical Program Manager, APAC

Sr Staff Clinical Technical Program Manager, APAC

Responsibilities

Requirements

Skills

Benefits

Sr Staff Clinical Technical Program Manager, APAC

Responsibilities

Requirements

Skills

Inhouse Clinical Research Associate - SA

Responsibilities

Skills

Benefits