In-Demand Clinical trial coordinator Jobs

Regulatory Submissions Coordinator - Entry
Medpace, Inc. —South Yarra VIC
- Full-time
- Research
- Microsoft Office
- Bachelor's degree
- Annual leave
7h
Clinical Trials Associate
University of the Sunshine Coast —Buderim QLD
- $82,843 - $93,358 a year
- Full-time
- Microsoft Office
- Databases
- Business
- Employee assistance program
5h
Occupational Therapist – Subcontractor Role
The Care Team Network —Melbourne VIC
- $90 - $120 an hour
- Contract
- Hybrid work
- Bachelor's degree
- First Aid Certification
- Professional development assistance
- Referral program
Quick Apply
8d
Occupational Therapist
Anglicare Southern Queensland —Hervey Bay QLD
- Full-time
- CPR Certification
- Clinic
- First Aid Certification
- Health insurance
- Employee assistance program
Prostate Cancer Specialist Nurse
Icon Group —Central Coast NSW
- Part-time
- Leadership
- Communication skills
- Nursing
- Parental leave
- Employee assistance program
Clinical Trial Coordinator
Alfred Health —Australia
- Full-time
- Management
- Working with children
- Communication skills
12d
Clinical Research Associate II/III - QLD
Novotech —Australia
- Full-time
- Hybrid work
- Patient monitoring
- Research
- Time management
- Parental leave
Clinical Research Associate - VIC
Novotech —Australia
- Full-time
- Hybrid work
- Nursing
- Patient monitoring
- Bachelor's degree
- Parental leave
Clinical Research Associate II/III - Perth
Novotech —Australia
- Full-time
- Nursing
- Patient monitoring
- Bachelor's degree
- Parental leave
13d
Physiotherapist- Full time
Pinarc Disability Support —Australia
- $96,965 - $140,524 a year
- Full-time
- Bachelor's degree
- Paediatrics
- Relocation assistance
- Parental leave

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Regulatory Submissions Coordinator - Entry

Medpace, Inc. -
South Yarra VIC

Apply Now

Job Details

Full-time | Contract
7 hours ago

Benefits

Annual leave

Qualifications

Research
Microsoft Office
Bachelor's degree
Communication skills

Full Job Description

Job Summary :

We are currently seeking a full-time, office based Entry level Regulatory Submissions (Study Start up) Coordinator to join our Clinical Operations team in the Australia, Melbourne office. This role is a vital part of the team to accomplish tasks and projects that are instrumental to the company’s success. If you are interested in an exciting career where you can use your expertise and develop and grow your career even further, then this is the opportunity for you.

Our culture is of expertise, and we empower our teams to employ their unique talents and experience to take an assertive approach to research, problem solving, and ultimately supporting our business partners. At Medpace, our employees embody our values and our approach to serving our clients. They work hard, understand our high expectations, and rise to the challenge. In return they are rewarded with interesting projects, career advancement, and recognition and exposure to our international footprint. These are just a few reasons why talented individuals join the Medpace team.

Responsibilities :

Perform required activities within the country that lead to activation of investigative sites in all phases of clinical trials;
Prepare, review, and submit to Regulatory Agencies (TGA / Medsafe);
Communicate with global study teams and personnel on study progress;
Ability to effectively identify risks to site activations and mitigate as necessary;
Provide expertise and guidance to global study teams in ethics and regulatory submissions;
Review and finalize essential documents required for site activation;
Act as a main contact for Ethical and Regulatory submission-related activities;
Direct contact with investigative sites during the study start up and activation process;
Ensure submissions comply with applicable regulations and guidance documents;
Advise sponsors on changing regulations and compliance requirements; and
Track submissions and ensure timely filing of documents.

Qualifications :

Bachelor's degree in the science field or equivalent combination of education and experience;
At least 1 year of relevant working experience at a CRO, Pharmaceutical Company, or an investigative site;
Experience in preparing and submitting TGA regulatory applications;
Excellent organization and communication skills;
Knowledge of Microsoft® Office;
Knowledge of ICH - GCP guidelines and regulatory guidelines in Australia and New Zealand;
Hands-on experience preparing, reviewing, and submitting regulatory documentation to Ethics Committees and Regulatory Agencies; including formulating responses to queries; and
Proactive approach to role with ability and willingness to learn and be challenged.

Medpace Overview :

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.

Why Medpace? :

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Medpace Perks

Flexible work environment
Competitive compensation and benefits package
Competitive PTO packages
Structured career paths with opportunities for professional growth
Company-sponsored employee appreciation events
Employee health and wellness initiatives

Awards

Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

Apply Now

Refine Your Search

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Regulatory Submissions Coordinator - Entry

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Clinical Trial Coordinator

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