Clinical Trial Associate, Oncology, EMEA
3 weeks ago
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
We are seeking a detail-oriented and highly motivated Clinical Trials Associate to join our oncology research team. As a Clinical Trials Associate in Oncology, you will play a crucial role in supporting the planning, coordination, and execution of clinical trials within the oncology portfolio. This role will require onsite presence a minimum of 3 days a week, in either of our California, New York or New Jersey offices to ensure effective global clinical trial management.
About You
You play a key role in supporting the planning, coordination, and execution of clinical trials within the oncology portfolio. Your primary responsibilities will include ensuring regulatory compliance, maintaining trial documentation, and facilitating effective communication among cross-functional teams. 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, including study protocols, informed consent forms, case report forms (CRFs), and other trial-related materials
* Collaborate with cross-functional teams to ensure accurate and timely completion of study start-up activities, such as site selection, feasibility assessments, and ethics committee submissions
* Support the organization and conduct of investigator meetings, study initiation visits, and other trial-related meetings
* Coordinate and track the distribution, collection, and reconciliation of trial supplies, investigational products, and study related materials
* Assist in the review and resolution of data queries, ensuring data accuracy and completeness within electronic data capture (EDC) systems
* In collaboration with TMF Operations team, maintain trial master files (TMFs) and study documentation in accordance with regulatory requirements and internal SOPs
* Facilitate effective communication among study team members, investigators, and study site personnel through regular correspondence and timely dissemination of study-related information
* Support the monitoring and tracking of study progress, including patient recruitment and enrollment, to ensure adherence to study timelines and milestones
* In collaboration with other Clinical Operations groups (Site Engagement and Monitoring Excellence) assist, as necessary, in the preparation and coordination of site monitoring visits, ensuring compliance with monitoring plans and resolution of site-related issues
* Stay updated with relevant regulations, guidelines, and industry best practices pertaining to oncology clinical trials, ensuring compliance, and implementing necessary changes as required.
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).
* 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.
* Ability to work onsite at least 3 days a week.
* Knowledge of one European languages and fluency in English (strong reading, writing, and speaking skills and an ability to effectively communicate with colleagues and stakeholders at all levels) is desired.
At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including:
* 401k plan with company matching
* Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)
* Mental health and wellness benefits
* Weeklong summer and winter holiday shutdowns
* Generous paid time off and holiday policies
* Life/AD&D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&D policies
* Enhanced parental leave benefit
* Daily subsidized lunch program when on-site
The expected salary range for this role is $100,000 to $109,250 depending on skills, competency, and the market demand for your expertise.
Eikon is proud to be an equal opportunity employer and will consider all qualified applicants for employment.
In accordance with the Company's duty to provide and maintain a safe workplace, the Company requires all employees to be Fully Vaccinated with one of the FDA approved COVID-19 vaccines, which includes those vaccines that have received the FDA's emergency use authorization. You will be expected to be Fully Vaccinated as of your Start Date. If you believe that you are exempt from this requirement under an applicable law or regulations, including Americans with Disabilities Act and California's Fair Employment and Housing Act, you will need to contact the Company's Human Resources group. For purposes of this section, Fully Vaccinated means (i) the completion of the vaccination regimen as approved by the FDA (by way of example, 2 doses of the Pfizer or Moderna vaccine and 1 dose of the Johnson and Johnson vaccine), and (ii) timely receiving booster vaccination, as recommended by the Centers for Disease Control and Prevention.
We are currently not accepting any new third-party agencies or firms at this time. Please do not forward unsolicited agency resumes to our website, employees or Human Resources. Eikon Therapeutics will not pay fees to any third-party agency or firm associated with unsolicited resumes.
-
Senior Clinical Research Associate
3 days ago
New York City, United States Worldwide Clinical Trials - USA Full timeWho we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications - from discovery to reality. Anchored in our company’s scientific heritage, our dedicated therapeutic focus on...
-
Senior, Clinical Trial Manager
2 days ago
New York, United States Argenx Full timeThe Senior Clinical Trial Manager (CTM) is responsible for all operational aspects of the assigned clinical studies from monitoring initiation till closure of the studies. The successful candidate will have clinical trial operational experience in phase I, II and III drug development phases and is an operational expert in the clinical trial activities from...
-
Clinical Trial Manager
2 months ago
New York, United States Cellectis Full timeJob DescriptionWHO WE ARE Cellectis is a global clinical-stage biopharmaceutical company. Pioneers and innovators in our field, our mission is to develop innovative treatments for patients with unmet medical needs. With 25 years of expertise, we have the best-in-class gene editing platform focusing on hematology oncology, solid tumors and gene therapy....
-
Clinical Trial Manager
4 weeks ago
New York, United States Cellectis Full timeJob DescriptionWHO WE ARE Cellectis is a global clinical-stage biopharmaceutical company. Pioneers and innovators in our field, our mission is to develop innovative treatments for patients with unmet medical needs. With 25 years of expertise, we have the best-in-class gene editing platform focusing on hematology oncology, solid tumors and gene therapy....
-
New York, New York, United States The US Oncology Network Full timeOverviewMedical Oncology Hematology Consultants, PA, an eight-physician oncology/hematology private practice is seeking a BC/BE medical oncologist/hematologist. We are a QOPI certified practice with strong clinical research-NCORP, Alliance, NRG, pharmaceutical trials, US Oncology Clinical Trials, and an ASCO Clinical Trials Award recipient. We provide up to...
-
New York, New York, United States The US Oncology Network Full timeOverviewMedical Oncology Hematology Consultants, PA, an eight-physician oncology/hematology private practice is seeking a BC/BE medical oncologist/hematologist. We are a QOPI certified practice with strong clinical research-NCORP, Alliance, NRG, pharmaceutical trials, US Oncology Clinical Trials, and an ASCO Clinical Trials Award recipient. We provide up to...
-
rn clinical trials coordinator 3
1 week ago
New Orleans, Louisiana, United States LSU Health Sciences Center Full timePosting Details Posting Summary Functional Position Title RN CLINICAL TRIALS COORDINATOR 3 Position Number Appointment Type Regular Location-City New Orleans School/Division MEDICAL SCHOOL Department Center of excellence-Cancer Position Summary The RN Clinical Trials Coordinator 3 (RN CTC3) will coordinate, manage, and assist physicians in enrolling and...
-
Clinical Trial Specialist
1 month ago
New Brunswick, United States Vitalief Full timeJob DescriptionJob DescriptionWHY VITALIEF?Vitalief is a pioneering consultancy addressing the healthcare human capital epidemic. Join us and help clients adapt to evolving requirements in the research and clinical trial industry with cutting-edge solutions. Reasons to Work for Vitalief:Our PEOPLE FIRST culture prioritizes personal and professional...
-
Clinical Trial Specialist
2 weeks ago
New Brunswick, United States Vitalief Full timeJob DescriptionJob DescriptionWHY VITALIEF?Vitalief is a pioneering consultancy addressing the healthcare human capital epidemic. Join us and help clients adapt to evolving requirements in the research and clinical trial industry with cutting-edge solutions. Reasons to Work for Vitalief:Our PEOPLE FIRST culture prioritizes personal and professional...
-
Clinical Trial Specialist
5 days ago
New Brunswick, United States Vitalief Full timeJob DescriptionJob DescriptionWHY VITALIEF?Vitalief is a pioneering consultancy addressing the healthcare human capital epidemic. Join us and help clients adapt to evolving requirements in the research and clinical trial industry with cutting-edge solutions. Reasons to Work for Vitalief:Our PEOPLE FIRST culture prioritizes personal and professional...
-
Clinical Research Nurse II
6 days ago
New York, United States NYU Langone Health Full timeWe have an exciting opportunity to join our team as a Clinical Research Nurse II - Oncology. Through the practice of professional nursing the Oncology Clinical Research Nurse (CRN) II prioritizes and advocates for the best interest of the patient enrolled on an oncology clinical trial while maintaining the fidelity of the clinical research protocol and...
-
Clinical Trial Manager
2 weeks ago
New York, United States INTRA-CELLULAR THERAPIES INC Full timeBenefits Offered 401K, Dental, Life, Medical, Vision Employment Type Full-Time “We deliver innovative treatments to improve the lives of individuals suffering from neuropsychiatric, neurologic and other disorders” Intra-Cellular Therapies Inc. is a publicly traded biopharmaceutical company headquartered in New York City. Founded on Nobel-prize...
-
Clinical Trial Manager
1 month ago
New York, United States Intra-Cellular Therapies, Inc Full timeBenefits Offered 401K, Dental, Life, Medical, Vision Employment Type Full-Time "We deliver innovative treatments to improve the lives of individuals suffering from neuropsychiatric, neurologic and other disorders" Intra-Cellular Therapies Inc. is a publicly traded biopharmaceutical company headquartered in New York City. Founded on Nobel-prize winning...
-
Clinical Trial Manager
4 weeks ago
New York, United States Intra-Cellular Therapies, Inc Full timeBenefits Offered 401K, Dental, Life, Medical, Vision Employment Type Full-Time "We deliver innovative treatments to improve the lives of individuals suffering from neuropsychiatric, neurologic and other disorders" Intra-Cellular Therapies Inc. is a publicly traded biopharmaceutical company headquartered in New York City. Founded on Nobel-prize winning...
-
Associate Clinical Trial Manager
2 weeks ago
New York, United States Lupus Research Alliance Inc. Full time**Associate Clinical Trial Manager, Lupus Therapeutics (Contract basis)** **Location**: Remote **Remuneration**: $100/hour, up to 25 hours per week **Background** The Lupus Research Alliance (LRA) is the world’s leading non-governmental, non-profit funder of lupus research. Over the past 20 years, the LRA has invested over $250 million in lupus...
-
Clinical Trial Associate
2 weeks ago
New Brunswick, United States Allen Spolden Full timeJob DescriptionThe remote-based Clinical Trial Associate (CTA) will perform tasks related to supporting operational strategy and and execution of clinical studies, supporting the strategy as defined in the Clinical Development Plan.Provide support for essential daily clinical study activities, including regulatory inspection readiness, following established...
-
Clinical Trial Manager
1 month ago
New York, United States BioSpace Full timeJob DetailsBenefits Offered401K, Dental, Life, Medical, VisionEmployment TypeFull-Time"We deliver innovative treatments to improve the lives of individuals suffering from neuropsychiatric, neurologic and other disorders"Intra-Cellular Therapies Inc. is a publicly traded biopharmaceutical company headquartered in New York City. Founded on Nobel-prize winning...
-
Clinical Trial Manager
3 weeks ago
New York, United States BioSpace Full timeJob DetailsBenefits Offered401K, Dental, Life, Medical, VisionEmployment TypeFull-Time"We deliver innovative treatments to improve the lives of individuals suffering from neuropsychiatric, neurologic and other disorders"Intra-Cellular Therapies Inc. is a publicly traded biopharmaceutical company headquartered in New York City. Founded on Nobel-prize winning...
-
Clinical Trial Specialist
1 month ago
New Brunswick, United States Vitalief Full timeWHY VITALIEF?Vitalief is a pioneering consultancy addressing the healthcare human capital epidemic. Join us and help clients adapt to evolving requirements in the research and clinical trial industry with cutting-edge solutions. Reasons to Work for Vitalief:Our PEOPLE FIRST culture prioritizes personal and professional growth for all Vitalief...
-
Clinical Trial Specialist
4 weeks ago
New Brunswick, United States Vitalief Full timeWHY VITALIEF?Vitalief is a pioneering consultancy addressing the healthcare human capital epidemic. Join us and help clients adapt to evolving requirements in the research and clinical trial industry with cutting-edge solutions. Reasons to Work for Vitalief:Our PEOPLE FIRST culture prioritizes personal and professional growth for all Vitalief...
