Senior Clinical Research Associate I/II

Avance Clinical; United States; Sur place; USD 80 000 - 120 000; Plein temps

Avantages offerts par ce poste

Stimulating work

Project diversity

Agile & flexible workplace

Opportunity to progress

Stability

Sense of community

Flexible work options

Great tools / tech to do your job

Résumé du poste

Avance Clinical is a CRO focused on drug development for pharmaceutical and biotech companies. We are seeking a Clinical Research Associate to monitor sites, ensure compliance with ICH GCP, and collaborate with investigators and sponsors on study deliverables.

You will conduct feasibility, manage monitoring visits, raise data queries, maintain TMF, and participate in audits. Travel up to 50% may be required; a life sciences degree and 3–4 years CRA experience are required.

Qualifications

• Proven ability to communicate effectively in writing and verbally with sponsors and sites.
• Strong problem-solving and decision-making abilities under pressure.
• Awareness of privacy legislation as it applies to clinical trials.

Responsabilités

• Conduct site and investigator feasibility activities.
• Coordinate HREC submission requirements to completion.
• Develop study-related documents under supervision of the Project Manager.
• Oversee multi-site study operations as Lead CRA including monitoring plan and reports.
• Perform on-site and remote PSV, SIV, DWV, IMV and COV visits.
• Generate/maintain high-quality site documentation and QA letters.
• Monitor data queries and resolve discrepancies with site staff.
• Ensure TMF/document filing per SOPs and protocol.
• Maintain proactive site communications and issue management.
• Support audits and respond to observations as required.
• Ensure SAE reporting per protocol requirements.
• Mentor less experienced staff during monitoring visits.

Connaissances

Written & verbal communication

Problem solving

Travel flexibility

Confidentiality awareness

Formation

Bachelor's degree in life sciences, pharmacy, nursing, or equivalent

Description du poste

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 1980's. 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.

We are committed to creating a flexible work environment for our people by supporting them to balance their work commitments and personal needs, both now and into the future.

Broad Purpose

Avance Clinical is a Contract Research Organisation which offers specialised services supporting drug development for the pharmaceutical and biotechnology industry.

Core Responsibilities

• Conduct site and investigator feasibility activities.
• Coordinate Human Research Ethics Committee submission requirements to completion.
• Develop study-related documents or plans under the supervision of the study Project Manager.
• For a multi-site study, oversee and lead the operations of the clinical team as the Lead CRA including development of Clinical Monitoring Plan, study-specific annotated report, reviewing Visit Reports.
• Perform all activities (preparation, execution, and follow-up) associated with onsite or remote Pre-Study Visits (PSV), Study Initiation Visits (SIV), Dose Witness Visits (DWV), Interim Monitoring Visits (IMV) and Close-out Visits (COV).
• Generate and maintain high quality confirmation letters, site visit reports, follow-up letters and other documentation related site monitoring and management to ensure compliance with ICH GCP, study protocol and regulatory requirements.
• Monitor participant source data, review Investigator Site Files (ISF), perform Investigational Product accountability, meet with site personnel, and ensure procedures are conducted in accordance with the protocol and ICH GCP.
• Perform protocol review as requested.
• Raise data queries in the Case Report Form (CRF) where discrepancies are identified and work with site staff to ensure timely and accurate resolution.
• Collect TMF documentation from site and ensure accurate and timely filing as per SOP requirements.
• Maintain effective site communication to proactively manage on-going study expectations and issues.
• 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 staff during co-monitoring visits and facilitating accompanied site visits.
• Other duties as directed by Line Management or delegate in line with skills, experience and/or qualifications.

Departmental Responsibilities

• Foster the on-going commitment to maintaining a healthy team culture and promoting good morale, by actively participating in regular Clinical Operations Team meetings.
• Maintain effective communication with other members of the department.
• Proactively identify risks related to departmental service provision and assist in their mitigation and resolution.
• Manage and track business related expenses as per company policy.
• Identify training needs of the Clinical Operations Team and provide recommendations for appropriate training actions and programs.
• Contribute to the development of departmental SOPs as required.
• Participate in internal Quality Assurance activities as required, including responding to internal audit findings.

Organisational Responsibilities

• Embrace the core values of Avance Clinical and endeavour to display those attributes at all times with clients and staff alike.
• Commit to Avance Clinical training programs.
• Adhere to Avance quality systems.

All staff are required to take reasonable care for their own health and safety and that of other personnel who may be affected by their conduct.

The accountabilities as specified above may be altered in accordance with the changing requirements of the position.

Qualifications, Skills, And Experience

• Bachelor's level degree in life sciences, pharmacy, nursing, or equivalent field.
• Previous experience as a CRA in a CRO or Pharma company for at least 3-4 years.
• Formal ICH GCP training and a working knowledge of ICH GCP Guidelines and other 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.
• Awareness 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. Moderate level of interstate travel may be required (up to 50%).

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