Join our expanding business. Experienced Project Associate required - exciting growth opportunity.
23rd September, 2024
Senior Project Associate required for our growing business.
Please note this is a full time office based position.
Who are we?
We're Avance Clinical a Contract Research Organisation. We offer specialised services supporting drug development for the pharmaceutical and biotechnology industry. We have a rich history in this area with our founding roots dating back to the 1980s. If you already work in this industry, you'll know that we are experts in our field.
Why should you join Avance Clinical?
We appreciate that our most important asset is our people. We offer a fun, friendly work environment and a culture that values honesty and respect. We have a strong sense of team. We genuinely appreciate each individual but recognise the collective when achieving success ...all in a fast-paced, positively evolving organisation that also offers excellent career progression.
The role
The Senior Project Associate (Snr PA) works alongside the Project Manager (PM) to plan and execute projects, coordinating staff and processes to deliver projects on time, within budget and with the desired outcomes while ensuring the trial is conducted in accordance with the protocol, company Standard Operating Procedures (SOPs), ICH GCP guidelines and other applicable regulatory requirements. The Snr PA may also act as the Project Lead on less complex projects.
Core Responsibilities include:
With minimal oversight by the respective PM, supports all aspects of project delivery from study commencement to completion, including:
Establish and configure project management systems, processes and trackers during the initiation phase of a study.
Draft Kick-Off Meeting materials and liaise with all stakeholders to facilitate the meeting.
Draft project plans for review by the Project Manager.
Maintain project information in the Clinical Trial Management System (CTMS), including project milestone tracking.
Accurately track project action items, risks, and issues.
Organise, facilitate, create agendas and take minutes for project/study team meetings.
Lead internal and external project/study team meetings.
Liaise with cross-functional team members to ensure good communication across each study.
Trial Master File (TMF) document review, metadata update and management.
Facilitate quarterly reviews of the TMF with the PM.
Track vendor invoices, site invoices, and investigator grants payments on assigned projects.
Assist the PM with monthly revenue recognition and forecasting, and review customer invoices for project labour and expenses.
Key Performance Indicator (KPI) tracking and reporting to Sponsor.
Source, supply (shipping and tracking), and maintain drug/study supplies.
In-house contact for administrative protocol queries, and study related questions.
Participate in study-specific or vendor audits conducted by sponsors or regulatory agencies, and respond to audit observations, as required.
Ensure Serious Adverse Events are reported (initial and follow-up) as per protocol requirements.
Provide guidance and mentoring to less experienced project management staff members.
Qualifications, Skills and Experience
Bachelor's level degree in life sciences, pharmacy, nursing, or equivalent field (highly regarded), or appropriate industry experience.
Previous experience as a PA (or equivalent) in a CRO or Pharma company for at least 2 years.
Previous experience as a Clinical Trial Assistant (or equivalent) is highly regarded.
Working knowledge of ICH GCP Guidelines and applicable regulatory requirements.
Clear understanding of the requirement to adhere strictly to client confidentiality.
Effective written and oral communications skills, including the ability to keep clients, senior management and other stakeholders informed of project updates and other pertinent information.
Demonstrated ability to take initiative in problem solving and in exercising good judgment.
An understanding of Privacy Legislation as it applies to the Clinical Trial Environment.
Ability to work under pressure in a multi-disciplinary team environment.
Willingness to work in, and be supportive of, a positive and dynamic team culture.
Ability to travel (desirable). Very minimal level of travel may be required (up to 10%).
What we offer
Stimulating work
Project diversity
An intellectual challenge
An agile & flexible workplace
Opportunity to progress
Stability
Sense of community
A leadership team that are working together on a common goal
Flexible work options
Great tools / tech to do your job
A competitive salary & an extra days holiday for your birthday!
What next?
As a growing business we're looking for likeminded people to join us – we hope that's you.
To join our team please submit your CV & cover letter as one Microsoft Word document
You must have full Australian working rights to be considered
At Avance difference is encouraged, it's celebrated and it's something we strive for. We empower cultural, disability, LGBTI+, and gender equality.
#J-18808-Ljbffr
