1

Study Start Up Associate Jobs in Connecticut (NOW HIRING)

Provide on-site assistance during system start-up and commissioning * Remote and on-site customer support * Assist Sales with pre-study analysis and reports * Interact with customers as required

Automation Warehouse Associate

Suffield, CT · On-site

$15.50 - $18.50/hr

Automation Warehouse Associate RugPadUSA is a growing e-commerce business looking to find ambitious ... Lead daily line start-up: verify safety checks, correct materials, labels, and settings; confirm ...

Stifel is more than 130 years old and still thinking like a start-up. We are a global wealth ... associates, among hundreds more. Let's talk about how you can find your place here at Stifel, where ...

Client Service Associate

Hamden, CT · On-site

$44K - $65K/yr

About Stifel Stifel is more than 130 years old and still thinking like a start-up. We are a global ... associates, among hundreds more. Let's talk about how you can find your place here at Stifel, where ...

Stock Associate, PT - 5am Start

Clinton, CT · On-site

$14.75 - $18.75/hr

As a Stock Associate, you're the engine behind our store's energy - keeping shelves stocked ... Can stand, lift, walk, bend and lift cartons weighing up to 25 lbs./12 kgs during each work shift ...

About Stifel Stifel is more than 130 years old and still thinking like a start-up. We are a global ... associates, among hundreds more. Let's talk about how you can find your place here at Stifel, where ...

Sign up associates and provide study material for any applicable ASE certifications * Proper ... Manages daily preparation of location, service desk, and equipment prior to start of business each ...

Showing results 41-60

Study Start Up Associate information

See Connecticut salary details

$12

$30

$52

How much do study start up associate jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for study start up associate in Connecticut is $30.00, according to ZipRecruiter salary data. Most workers in this role earn between $20.14 and $39.57 per hour, depending on experience, location, and employer.

What is the difference between Study Start Up Associate vs Clinical Trial Coordinator?

AspectStudy Start Up AssociateClinical Trial Coordinator
Required CredentialsBachelor's degree, knowledge of regulatory requirementsBachelor's degree, familiarity with clinical procedures
Work EnvironmentRegulatory and site initiation activitiesParticipant management and site coordination
Employer & Industry UsagePharmaceuticals, biotech, CROsHospitals, research centers, CROs

The Study Start Up Associate primarily focuses on regulatory submissions, site qualification, and initiation processes, ensuring trial readiness. In contrast, the Clinical Trial Coordinator manages participant recruitment, scheduling, and data collection. Both roles are essential in clinical research but differ in their core responsibilities and focus areas.

What are popular job titles related to Study Start Up Associate jobs in Connecticut?

For Study Start Up Associate jobs in Connecticut, the most frequently searched job titles are:

What job categories do people searching Study Start Up Associate jobs in Connecticut look for?

The top searched job categories for Study Start Up Associate jobs in Connecticut are:

What cities in Connecticut are hiring for Study Start Up Associate jobs?

Cities in Connecticut with the most Study Start Up Associate job openings:

Infographic showing various Study Start Up Associate job openings in Connecticut as of August 2026, with employment types broken down into 1% As Needed, 64% Full Time, 15% Part Time, 2% Temporary, and 18% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $62,408 per year, or $30 per hour.

Technical Clinical Data Manager /Data Analyst (Remote)

Penfield Search Partners

Fairfield, CT • Remote

Full-time

Re-posted 3 days ago


Job description

Job Description Contact: Neisha Camacho/Terra Parsons - teamnt@penfieldsearch.com No 3rd party candidates We are partnering with a growing biotech organization seeking a Clinical Data Manager/Data Analyst to support ongoing and upcoming clinical programs across multiple therapeutic areas. This role will sit within a highly collaborative clinical development team and is ideal for a hands-on, analytical Clinical Data Manager who enjoys digging into the data, identifying trends or issues proactively, and developing creative solutions to improve data quality and study execution. The client is seeking someone resourceful and technically curious - not just process-oriented - with the ability to independently explore datasets, generate meaningful reports, and surface potential issues early

The ideal candidate will bring a blend of traditional clinical data management expertise along with strong data review, querying, and analytical skills. Experience with R, SQL, SAS, or other data interrogation and reporting tools is highly desirable. Key Responsibilities Support clinical data management activities across studies from start-up through database lock Perform hands-on data review and exploratory analysis to identify data trends, inconsistencies, missing data patterns, and potential study risks Develop custom reports, listings, and data visualizations to support proactive data cleaning and study oversight Utilize R, SQL, SAS, or similar tools to query, analyze, and troubleshoot clinical datasets Partner with CROs and vendors to ensure high-quality, timely data delivery Collaborate cross-functionally with Clinical Operations, Biostatistics, Statistical Programming, Medical, and Safety teams on data review strategies and issue resolution Contribute to development and review of key deliverables including: Data Management Plans (DMPs) eCRF design and completion guidelines Edit checks and query logic User Acceptance Testing (UAT) Data review plans and cleaning processes Support ongoing query management and ensure data integrity, consistency, and inspection readiness Assist with implementation of data standards, reporting enhancements, and process improvements Work independently to investigate data anomalies and recommend practical solutions in a fast-paced biotech environment Qualifications BS in a scientific, technical, or clinical discipline Approximately 5-8 years of clinical data management experience within biotech, pharma, or CRO environments Strong hands-on experience reviewing and interrogating clinical trial data Experience using R, SQL, SAS, or other querying/reporting tools to analyze clinical data and generate custom reports Experience with EDC systems such as Medidata Rave, Oracle, or Veeva Working knowledge of CDISC standards (SDTM/ADaM) and downstream data usage Experience supporting Phase II and/or III clinical trials; CNS experience is a plus Exposure to CRO/vendor oversight Understanding of clinical data structures and dictionaries including MedDRA and WHODrug Strong critical thinking and problem-solving skills with the ability to work independently Resourceful, proactive, detail-oriented, and comfortable operating in a dynamic biotech environment Strong communication and cross-functional collaboration skills.