Study Start Up Associate
Impactful work. Meaningful Careers. Quality Rewards.
Join our team as a Study Start Up Associate and play a pivotal role in ensuring the smooth initiation of clinical trials at our research sites.
As a member of the Study Start Up Team, you will be responsible for conducting feasibility studies, identifying suitable research sites, negotiating contracts, and facilitating various Study Start Up activities. Responsibilities will also include coordinating submissions to regulatory and ethics bodies, as well as developing and reviewing subject information sheets and informed consent forms.
If you're ready to make a meaningful impact in the field of clinical research, apply now to join our dedicated Study Start Up team!
I’ve been working at ICON for almost 2 years now. I’ve been in the industry of clinical research for almost 20 years. Here at ICON I feel truly part of a community since the first day I joined the company, I feel valued and recognized. This company really embraces work life balance, diversity, and the People leaders are very supportive. If you care about people, if you want to make a difference on World Healthcare Intelligence, I invite you to apply to ICON. I’m pretty sure you’ll find a strong career path!
Senior Site Activation Lead
Roles in this area at ICON
Mexico City
Study Start Up
Remote Working
Business Area
ICON Strategic Solutions
Job Categories
Description
As a Site Activation Partner/ Study Start Up Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.Providing innovat
2024-115786
Expiry date
US, Lenexa KCI (PRA)
Full Service - Early Clinical and Bioanalytical Solutions
Office Based
ICON Full Service & Corporate Support
Temporary Employee
We are currently seeking a Clinical Trial Recruitment Representative to join our diverse and dynamic team. As a Clinical Trial Recruitment Representative at ICON, you will play a pivotal role in desig
US, Salt Lake City (PRA)
Salt Lake City
We are currently seeking a Clinical Trial Recruitment Representative to join our diverse and dynamic team at ICON at our Salt Lake City UT site. This is a PRN (as needed) role. Location: On-Site Salt
The Study Start-Up Associate performs investigative site recruitment/feasibility, essential document collection and review, clinical status tracking, and in-house site management activities in accord
2024-115530
United States
As a Lead Site Activation Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
2024-114527
Mexico, Mexico City
Hybrid: Office/Remote
At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own I
Brazil, Sao Paulo
Site Activation
The Sr. Study Start-Up Associate (Sr. SSUA) performs investigative site recruitment/feasibility, essential document collection and review, clinical status tracking, and in-house site management activi
2024-113196
India, Chennai
We are currently seeking a Due Diligence Specialist II to join our diverse and dynamic team. As a Due Diligence Specialist II at ICON, you will play a pivotal role in supporting the assessment and eva
Korea, South
South Korea
Home-Based, Seoul, South Korea As a (Study Start Up Associate I, II) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
2024-114764
We are currently seeking a Site Activation Lead to join our diverse and dynamic team. As a Site Activation Lead at ICON, you will advance clinical trial start-up activities by understanding client obj
Netherlands, Groningen GRQM
Zonder geneesmiddelenonderzoek geen nieuwe medicijnen, en zonder deelnemers geen geneesmiddelenonderzoek. Wil jij bijdragen aan de ontwikkeling van nieuwe en betere medicijnen, en daarmee patiënten ee
Impactful work. Meaningful careers. Quality rewards.
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Study Start Up Specialist / Lead
About the Opportunity
We are currently partnered with a clinical-stage Biopharmaceutical company that specializes in developing innovative cancer treatments. As the company looks to advance their robust pipeline, they are looking for an experienced Study Start-Up Specialist/Lead to join their expanding Clinical Operations team. This is a fully remote / permanent opportunity directly with a rapidly growing sponsor.
The annual base salary range is $100,000 to $125,000. Actual compensation offered to the successful candidate may vary from posted hiring range based upon geographic location, work experience, education, and/or skill level, among other things. Details about eligibility for bonus compensation (if applicable) will be finalized at the time of offer.
Job Responsibilities
- The Study Start-Up Specialist/Lead is accountable for the execution of the study start-up strategy and planning, including the management and coordination of start-up activities such as alignment to US regulations, Core/Site document collection/ approval, ICF customization/approval, SIV scheduling and activation requirements
- Coordinate essential documents collection with study sites in accordance with local processes
- Coordinate the Feasibility activities
- Coordinate the identification and selection of research sites
- Create, maintain/track, and obtain approval on essential study start up documents
- Assist with activities relating to identification vendors as applicable
Job Requirements
- Bachelor’s Degree with 3+ years of clinical research experience at a pharmaceutical company, Biotech or CRO
- Detailed understanding of clinical trial process across Phases I-II and ICH GCP
- Extensive knowledge of the top US oncology site’s start up process
- Ability to understand clinical protocols and associated study specifications
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Clinical Research Study Startup jobs. Sort by: relevance - date. 5,000+ jobs. Clinical Research Coordinator. New. Confidential. Richmond, VA 23237. From $55,000 a year. Full-time. Monday to Friday. Easily apply. ... For all clinical research studies assigned, the Clinical Research Coordinator (CRC) is responsible for coordinating clinical ...
Clinical Study Startup jobs. Sort by: relevance - date. 100+ jobs. Data Ops Engineer. ... To that end, we build a cutting-edge software suite that connects all clinical research stakeholders, from research teams to treating physicians, patients, and study sponsors on a real-time, real-world data SaaS platform, powered by AI.
Description. JOB SUMMARY. The Research Specialist provides support in the design and implementation of research strategies for clients, clinical trial programs and studies.The Research Specialist performs administrative and supportive activities to ensure the contracted services and expectations are carried out by the project team in accordance with executed contracts and the customers ...
Join our team as a Study Start Up Associate and play a pivotal role in ensuring the smooth initiation of clinical trials at our research sites. As a member of the Study Start Up Team, you will be responsible for conducting feasibility studies, identifying suitable research sites, negotiating contracts, and facilitating various Study Start Up ...
Given this is a start-up, the site director will serve as the primary Clinical Research Coordinator (CRC) until a team is hired. The Site Director will continue to act as a working manager, providing backup support for CRCs as needed, including consenting patients, taking vitals, performing ECGs, and other trial-related duties.
Coordinate the identification and selection of research sites; Create, maintain/track, and obtain approval on essential study start up documents; Assist with activities relating to identification vendors as applicable . Job Requirements. Bachelor's Degree with 3+ years of clinical research experience at a pharmaceutical company, Biotech or CRO
In Study Start Up (SSU) we support the start-up process and manage the critical path to site activation. SSU is one of the most complex and heavily regulated parts of any clinical trial or program launch. This period involves a significant number of stakeholders at start-up sites, regulatory agencies, vendors as well as the customer.
Browse 179 CLINICAL RESEARCH STARTUP jobs ($81k-$150k) from companies with openings that are hiring now. Find job postings near you and 1-click apply! Skip to Job Postings. Jobs ... Coordinate studies from startup through close-out * Develop and manage data collection processes Report Job. Senior Director, Clinical Trial Startup & Amendments ...
About the role: The Study Start-Up CRA is accountable for site selections as well as study-specific start-up activities and deliverables of assigned sites for Phase I-IV GDD trials within the country in adherence with monitoring procedures and processes in accordance with ICH/GCP, local regulations and SOPs.
60 Clinical Research Study Start Up jobs available on Indeed.com. Apply to Research Scientist, Liaison, Clinical Research Coordinator and more!