Clinical Trial Associate at Eikon Therapeutics, candidates with BS degree can apply!
About Eikon Therapeutics: Eikon Therapeutics is a new biopharmaceutical company employing revolutionary technology at the intersection of chemistry, engineering, computation, and biology to discover novel treatments for life-threatening diseases. Eikon’s discovery platform is built on groundbreaking innovations from its founders (Nobel Prize, 2014), culminating in the creation of microscopes which enable real time, molecular-resolution measurements of protein movement in living cells, thereby unlocking otherwise intractable classes of proteins as drug targets.
Position: Clinical Trial Associate, Oncology
Location: Millbrae, CA; Jersey City, NJ; New York, NY
Description: As a Clinical Trials Associate in Oncology, you will play a crucial role in supporting the planning, coordination, and execution of Phase I-III insourced global clinical studies within the oncology portfolio. Operating in a dynamic and collaborative environment, you will provide essential support for the execution of clinical trials, contributing to the development of groundbreaking therapies with the potential to transform patient lives.
About You: You are passionate about playing a key role in supporting the planning, coordination, and execution of clinical trials within the oncology portfolio. You have strong communication skills and a passion for advancing care to patients.
What You’ll Do:
- Assist in the preparation and maintenance of essential study documents.
- Collaborate with cross-functional teams for study start-up activities.
- Support investigator meetings and trial-related meetings.
- Coordinate and track distribution of trial supplies.
- Review and resolve data queries for data accuracy.
- Maintain trial master files and study documentation.
- Facilitate communication among study team members.
- Support study progress tracking and patient enrollment.
- Stay updated on regulations and best practices.
Qualifications:
- An Advanced Degree without experience or Bachelor’s degree with 2 years of experience in a relevant field (e.g., life sciences, healthcare, or related discipline)
- Ability to communicate in multiple languages (especially European languages) will be considered a strong asset
- Previous experience working as a Clinical Trials Associate, Study Coordinator, or in a similar role within the pharmaceutical, biotechnology, or CRO industry is preferred
- Knowledge of clinical trial regulations, guidelines, and best practices, including ICH-GCP and FDA requirements
- Strong organizational skills and attention to detail, with the ability to manage multiple tasks and prioritize workload effectively
- Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems
- Excellent written and verbal communication skills, with the ability to effectively interact with study team members and internal / external stakeholders
- Ability to work independently as well as collaboratively in a team-oriented environment
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Project)
- Adaptability and willingness to learn and embrace new technologies, processes, and industry trends
Employee Benefits:
- 401k plan with company matching.
- Medical, dental, and vision insurance covered by Eikon.
- Mental health and wellness benefits.
- Generous paid time off and holiday policies.
- Enhanced parental leave benefit.
- Competitive salary range: $104,000 to $114,000.
Eikon is proud to be an equal opportunity employer. We are not accepting third-party agencies/firms at this time.
Keywords: Clinical Trial Associate, Oncology, Eikon Therapeutics, New York, New Jersey, California, Clinical Trials, Phase I-III, FDA, ICH-GCP
