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Clinical Research Associate II

Work from home

Remote role where the employee must remain based in a particular country.

Australia only

From the employer's advert: We’re searching for a knowledgeable, team-oriented CRA II to manage the clinical aspects of full-service global projects in Australia.

Employer listed it 3 weeks ago · Added 2 weeks ago

Been open since 3 weeks ago, still being checked, but it has been live a while.

Salary

Not stated

Location

Australia only

Timezone

APAC

Contract

Full-time

Experience

Entry

Category

Other

The employer did not publish a salary, and we have too few comparable roles to estimate one.

What the advert says

Quoted word for word from the employer's advert. Where it says nothing, we say so.

Working hours
Not mentioned in the advert
Where you can work from
Conduct and report all types of onsite monitoring visits
Contract
Not mentioned in the advert
Experience asked for
Not mentioned in the advert
Pay
Competitive salary

Remote flexibility

Work from home

This is a remote role, but the employee must be based in Australia. It is work from home rather than work from anywhere.

What the employer says

  • Source listing states candidate location: "Melbourne, VIC, Australia, Melbourne, VIC, au, Remote"

What Nomaders makes of it

  • Residency required in Australia
  • Payroll and tax are likely handled in that country only

The quotes above are the employer's own words; the reading is ours. Always check the original listing and employment terms before working from another country.

Before you apply

Experience: employer states

Written as a requirement

  • “At least 2 years of independent on-site monitoring experience in Australia”

Written as a nice-to-have

  • “Experience in Inflammatory Bowel Disease, Oncology, Infectious Diseases is a plus”

Questions worth asking: Nomaders interpretation

  • The advert does not say whether this is employment or a contractor arrangement. Ask, as it affects tax and benefits.

Produced automatically from this advert's text; not reviewed by a person. The employer's own page is the final word.

About the role

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do.  A dynamic, global company founded in 1995, we bring together 3000 driven, dedicated and passionate individuals.  We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

PSI’s business is about conducting clinical research of novel medications. We work at the interface of R&D, pharmaceutical industry and healthcare science and provide services to big and mid-sized pharmaceutical companies.  We help our clients to generate data about safety and efficacy of medications and bring the best ones to market.  By conducting global clinical research trials, PSI makes cutting-edge treatment available in drugstores all over the world and helps patients with serious medical conditions to improve or even save their life.  Help us to make sure that PSI medical and business documents are clear to patients, physicians, regulatory authorities, and clients.

We offer an inspiring story of the company that has grown organically from a handful of countries to global presence.  PSI is a mature company with standards and practices, but we do not stand still.  Every day, there is a figurative Everest to climb, and you will not get bored here.

We’re searching for a knowledgeable, team-oriented CRA II to manage the clinical aspects of full-service global projects in Australia. As a CRA II at PSI, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications.  You will build and maintain relationships with clinical sites and investigators.  You will focus on subjects’ rights, safety and well-being and quality of data compliance. 

You will:

Conduct and report all types of onsite monitoring visits

Be involved in study startup

Perform CRF review, source document verification and query resolution

Facilitate site budgets and contract negotiations

Monitor trial progress on the country level

Be responsible for site communication and management

Be a point of contact for in-house support services and vendors

Communicate with internal project teams regarding study progress

Participate in feasibility research

Support regulatory team in preparing documents for study submissions

College/University degree in Life Sciences, Pharmacy, RN or an equivalent combination of education, training & experience

At least 2 years of independent on-site monitoring experience in Australia

Experience in all types of monitoring visits in Phase II and/or III

Experience in Inflammatory Bowel Disease, Oncology, Infectious Diseases is a plus

Full working proficiency in English 

PC skills to be able to work with MS Word, Excel and PowerPoint

Ability to plan, multitask and work in a dynamic team environment

Communication, collaboration, and problem-solving skills

Ability to travel

Requirements

  • ·Ability to plan, multitask and work in a dynamic team environment
  • ·Communication, collaboration, and problem-solving skills
  • ·Ability to travel
  • ·What you’ll get:
  • ·Competitive salary

Benefits

  • ·Access to a wide range of employee benefits such as onsite Gym access
  • ·Additional 5 days of wellness leave
  • ·Development and learning opportunities
  • ·Chance to make a real impact in a meaningful industry
  • ·How are we different?

How to apply

  1. 1Check the flexibility label above, work from home, matches where you plan to live and work.
  2. 2Tailor your CV to the role at PSI CRO, mentioning your remote working experience and working hours (APAC).
  3. 3Apply directly on the employer's careers page using the button below. Nomaders never handles your application.

Found 17d ago. Last checked today. Always confirm the details on the original posting, salary and location can change after publication.

Listing sourced from Company boards.

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