Australia & ASIA PACIFIC CLinical oncology research development workshop | 22 - 27 SEPTEMBER 2024

MAGENTA SHORES, NSW, AUSTRALIA

MESSAGE FROM THE ACORD CONVENOR

2024 MARKS THE 20TH YEAR of the ACORD initiative and will be our ninth biennial 1-week Protocol Development Workshop to be held at The Pullman Magenta Shores, NSW. Over 500 early career clinical cancer researchers from 19 countries in the Asia Pacific have participated in our Protocol Development Workshops. Since 2004 over 600 others have participated in our half day Clinical Research Idea Starters’ Workshops, and 1-day Concept Development Workshops.

ACORD brings participants with new Research ideas together with local and international experts who provide the knowledge, skills, experience and global perspectives needed to develop high quality clinical cancer research. The Workshop uses problem-based, participant-centred, adult-learning principles including short, interactive lectures combined with small group, problem-oriented, protocol development sessions focusing on both clinical research methods, and on oncology sub-specialties. Participants also benefit from individual feedback from multiple experts as they develop their research protocols, and from the opportunity to establish ongoing, long term, research collaborations.

The ACORD initiative has been made possible by longstanding collaborations of the Medical Oncology Group of Australia (MOGA), the American Association for Cancer Research (AACR), the American Society of Clinical Oncology (ASCO), the National Cancer Institute of the United States (NCI), the Clinical Oncological Society of Australia (COSA), the Cancer Council of Australia (CCA), and Cancer Australia.

Our next ACORD Protocol Development Workshop is scheduled for 22 - 27 Sept 2024, at The Pullman Magenta Shores, New South Wales. It is shaping up to be our best!

  • Applications Open | 1 January - 29 February 2024 AEST* (CLOSED)

    *no late applications will be considered

    Offer of Places for Participants | 6 - 10 May 2024

    Faculty and Participant Orientation/Briefings | 6 September and 13 September 2024

  • Participants are required to commit to full-time participation in the 6-day Workshop program, all pre-Workshop online activities in the 2 weeks prior and to contribute to long term project evaluation.

    All selected participants are required to pay the Workshop Participation Fee of AUD$3,000.00 or AUD $600 (participants from low middle income countries - World Bank listing). Including 1.75% + A$0.30 for domestic cards and 3.5% + A$0.30 for international cards + 10% GST (for Australian transactions ONLY).

    The Workshop Participation Fee includes:

    • Exclusive access to and mentoring by highly experienced clinical experts in oncology;

    • Access to Workshop portal, the online resource platform for all Workshop material;

    • Accommodation at the Workshop venue from 22-27 September 2024;

    • Food and beverages throughout the duration of the Workshop;

    • Shuttle bus service from Sydney airport to the Workshop venue on Sunday 22 September 2024 and from the Workshop venue to Sydney airport on Friday 27 September 2024.

    PLEASE NOTE: Any additional and unauthorised travel expenses will not be reimbursed. Participants are responsible for their own return interstate or international airfares.

    Registration

    The link to the registration form will be sent to selected applicants in May 2024. Only fully completed online registrations will be accepted. The registration will only be confirmed upon receipt of full payment. If full payment is not received by the deadline, the Participant’s offer of a place will be withdrawn and provided to the next applicant on the waiting list.

    Methods of Payment

    Visa · American Express · Mastercard · eftpos Australia · Apple Pay · Google Pay.

    Cancellation & Refunds

    Registration fees are not refundable.

  • The Workshop Steering Committee will evaluate the applications and base its decision on a number of factors including:

    • Quality and feasibility of the proposed protocol concept and the letters of commitment submitted;

    • Individual career path in medical training and competence in clinical cancer research;

    • Support of relevant departments and/or institutions to help conduct the clinical trial.

    The selection of applications is at the sole discretion of the Workshop Steering Committee. Whilst feedback on the application process and selection is welcome, the Workshop Steering Committee will not enter into any discussions regarding the final decision. Applications will be accepted from those based in East Asia and Pacific regions.

    ELIGIBILITY CRITERIA

    ⦿ Applications will be accepted from cancer clinical researchers working in any oncology-related discipline, including medical, surgical or radiation oncology, palliative care, psycho-oncology, pathology, radiology, nuclear medicine, nursing, allied health, and others.

    ⦿ Preference will be given to applicants near the end of their clinical and/or research training, including fellows and recently registered specialists who completed training within the last 5 years.

    ⦿ Applicants from other professions involved in cancer research will be considered.

    ⦿ A limited number of applicants not based in the Asia Pacific may be accepted.

    ⦿ Be fluent in written and spoken English and have good computer skills.

    ⦿ Applicants are required to accept and comply with the ACORD 2024 Workshop Terms and Conditions as part of their application.

    ASSESSMENT CRITERIA

    ⦿ Quality and feasibility of the clinical research proposal.

    ⦿ Applicant’s commitment to participation in the workshop and evaluation.

    ⦿ Supervisor’s, institution’s and/or group’s commitment to support the proposed research.

    ⦿ Track records of the applicant, and of their supporting institution(s) and/or group(s): extent to which participation at the ACORD PDW will help the applicant, proposal and supporters succeed.

    ASSESSMENT PRINCIPLES

    ⦿ Reviewers rate applications on the promise (potential) of the proposed idea, applicant, and their local support

    ⦿ We are seeking for promising applicants, proposals and support that we can help succeed.

    ⦿ Applicants may have little or no track record in clinical research, but we are looking for promise which can also be manifested by evidence of interest, enthusiasm, inquisitiveness, etc. We also consider how beneficial workshop participation would be to the applicant’s clinical research career.

    ⦿ Proposed study. How good is the underlying idea and what are the prospects of turning this idea into a protocol for a study that is likely to be successful? Proposed studies are often over-ambitious and/or unsuitable as an applicant’s first ever study. However, we are looking for ideas that have the potential to be successful, perhaps with major simplification and/or scaling back. For example, the applicant might have proposed a large-scale phase 3 trial which is unlikely to be feasible, but a phase 2 trial assessing activity, or even a phase 1 trial assessing the intervention’s feasibility might be better, and more feasible.

    ⦿ Support of Supervisors, institutions, and groups range from world-leaders to neophytes: how strongly can/will they help the applicant? How much difference will the participant attendance at ACORD make to the supporting institution or group?

    SUPPORTING DOCUMENTATION

    ⦿ Concept outline for the proposed clinical research study. (download template)

    ⦿ Current 2024 curriculum vitae including a list of peer-reviewed publications.

    ⦿ Applicant’s letter including their background, career plans, reasons for attending the workshop, and assurances regarding participation in the workshop.

    ⦿ Letter of support from applicant’s supervisor, including a written assurance that reasonable efforts will be made to support the proposed clinical research project.


Participants & Faculty

 

Participants

THE WORKSHOP WILL INCLUDE participants selected based on the quality, potential, and originality of their proposed research project, and evidence of support from their supervisor, head of department, collaborative group, or senior co-investigators. Applicants from all oncology disciplines and backgrounds are welcome, including medical, surgical, radiation and psycho-oncology, haematology, palliative care, pathology, imaging, nursing and allied health.

Workshop participants work with their peers and receive individual guidance and assistance from the faculty to develop their idea for a clinical research study into a study protocol suitable for submission to a Human Research Ethics Review Committee or funding body.

Faculty

THE ACORD FACULTY WILL INCLUDE distinguished international experts in clinical cancer research and practice. Previous faculty members have included leading members of ASCO, AACR, ESMO, MOGA, national and international cooperative trials groups and major cancer centres in North America, Europe, Asia, Australia and New Zealand.

Recent Workshops have included future faculty fellows, selected from the Asia Pacific region, as emerging leaders in oncology trials and research, to further the development of their expertise as clinical research mentors.




Educational Format & Program

 

THE WORKSHOP PROGRAM comprises a mix of academic sessions ensuring that all learning needs are addressed, including:

Protocol Development Group Sessions

These sessions are a core activity and allow participants to complete their protocol by applying the knowledge acquired during the Workshop. Participants receive extensive feedback on their trial concepts from designated faculty within assigned groups comprising a maximum of 8-10 participants.

ACORD 2018 Workshop Participants and Plenary session with Prof Martin Stockler, Convenor ACORD 2018

Faculty Sessions

One-to-one sessions where participants have access to Workshop Faculty providing individual counselling on protocol related issues and advice on career development.

Small Group Discussion Sessions

Sessions that focus on topics that are essential to the development of clinical trials and facilitating discussion on the difficulties and challenges of a particular type of trial. Attendance at these sessions is limited to maximise interaction and information exchange.

Lectures and Panel Discussions

Presentations by key Faculty and experts on specific topics providing participants with an overview of the design and implementation of high-quality clinical trials. These are followed by a panel discussion during which Faculty, experts and participants explore issues raised during the talks in greater depth.

 

Location

 

ACORD WILL be held at Pullman Magenta Shores, located on the Central Coast of NSW, Australia. Magenta Shores is 90 minutes’ drive from the Sydney CBD and its many international flight connections. Transfers from Sydney will be available.

 

Collaborating Partners & Sponsors