Start-Up Associate

Description ¨ Collect, track and perform a quality review of all essential & investigator documents required for effective and compliant study site activation and maintenance¨ Ensure that all assigned maintenance and Start-up activities are on track and in accordance with client expectations, ICH/GCP, SOPs, budget, quality and applicable laws and guidelines¨ Serve as primary contact for investigative sites and ensure documents required are collected in a timely manner.¨ With guidance from line manager and experienced colleagues, adapt Informed Consent Forms and other patient facing material to country specific requirements.¨ May support / assist the contract negotiation process under supervision of an experienced colleague or line manager.¨ Escalate study issues appropriately and in a timely fashion.¨ Update study documents when there are changes in study personnel/study amendments.¨ Contribute to the preparation of submissions to IRB/IEC with appropriate supervision.¨ Ensure high quality documents are filed and systems are updated on an ongoing and timely basis making Covance ready for an audit at any time.¨ Undertake tasks delegated by senior team members, depending upon country and situational requirements with proper supervision.¨ Perform other duties as assigned by management.Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials.Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need.Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact.