- അനുഭവം
- ഏതെങ്കിലും
- ശമ്പളം
- USD 72,500 – USD 157,200 / year
- ഓപ്പണിംഗുകൾ
- 1
- പോസ്റ്റ് ചെയ്തു
- 1 ആഴ്ച മുമ്പ്
- പ്രവർത്തന രീതി
- വീട്ടിൽ നിന്ന് ജോലി ചെയ്യുക
- വിദ്യാഭ്യാസം
- Bachelor’s degree in Life Sciences or related scientific discipline
- പുനരാരംഭിക്കുക
- അപേക്ഷിക്കാൻ നിർബന്ധം
ജോലി വിവരണം
Role Overview
As an Internal Clinical Research Associate, you will be instrumental in supporting vital clinical trial processes from site activation through to study completion. Your role ensures adherence to regulatory standards, quality protocols, and clinical research best practices throughout the study lifecycle.
Key Responsibilities
- Assist in site selection, qualification, activation, ongoing monitoring, and study closeout activities across multiple clinical trials.
- Maintain Trial Master Files and essential documentation to guarantee readiness for inspections and compliance with regulations.
- Collaborate with clinical teams to prepare, review, and manage necessary study documents for effective trial implementation.
- Review and oversee informed consent forms, case report forms, and other trial-related materials to ensure accuracy.
- Prepare and distribute study newsletters and other communications to support investigative sites and cross-functional teams.
- Track and support invoicing processes related to clinical studies and keep associated documentation organized.
- Develop and update study metrics, reports, and dashboards to aid clinical trial monitoring and execution.
- Provide support for clinical trial registration, audit readiness, data collection efforts, and ensure adherence to Good Clinical Practice (GCP) and regulatory requirements.
Required Qualifications
- Bachelor’s degree in Life Sciences or a scientifically related discipline.
- No prior experience required; open to candidates starting their career.
Preferred Qualifications
- Background in clinical research, clinical trial operations, or clinical study management.
- Familiarity with Good Clinical Practice (GCP) guidelines.
- Experience using electronic clinical trial databases and clinical trial management systems.
- Knowledge supporting audit, inspection, and regulatory submission activities in clinical trials.
- Exposure to clinical trial registration platforms and study reporting operations.
Compensation and Benefits
- Annual salary ranges depending on location from $72,500 to $157,200 USD.
- Comprehensive health benefits including medical, prescription drug, dental, vision, critical illness, accident, and hospital indemnity insurances.
- Access to personalized healthcare support, wellbeing programs, and tobacco cessation support.
- Financial benefits such as Health Savings Account (HSA), Flexible Spending Accounts (FSAs), 401(k) plan, Employee Stock Purchase Plan (ESPP), life and AD&D insurance, and short-term disability coverage.
Additional Information
Stryker is a global leader providing innovative medical technologies across MedSurg, Neurotechnology, Orthopaedics, and Spine sectors, impacting over 150 million patients worldwide annually. Depending on client needs, employees or new hires in sales or field roles with customer interaction may be required to meet vaccination requirements as part of their job duties.