ZipRecruiter

Log In

1

Analytical Development Biotech Jobs in Connecticut

Artech Information System LLC

Scientist

Groton, CT

... development and mechanistic studies. Ability to work occasional weekends for clinical sample analysis is required. Previous pharma and/or biotech experience preferred. Please list out the (up to) top ...

LanceSoft Inc

Quality Engineer III

North Haven, CT

$71K - $92K/yr

... development process for the Pharmaceutical, Biotechnology, and Medical Device industries. We ... Perform failure analysis to prevent or correct component and product failures as well as other risk ...

Aequor

$115K - $138K/yr

... the biotechnology industry more than 40 years ago and remains on the cutting edge of innovation ... Automation, Data Analytics, Software Development, Supply Chain Systems, or a related field.

Artech Information System LLC

Scientist

Groton, CT

... development and mechanistic studies. Ability to work occasional weekends for clinical sample analysis is required. * Previous pharma and/or biotech experience preferred. Please list out the (up to ...

Tunnell Consulting

Senior Cost Accountant

Stamford, CT · On-site

$94K - $118K/yr

... cost development and variance analysis * Support physical inventory counts and cycle counts ... biotech/pharma a plus) * Strong knowledge of manufacturing, inventory, and cost accounting

System One

Scientist II

Ridgefield, CT · On-site

$35 - $40.05/hr

Perform quantitative analysis of histology, immunohistochemistry (IHC), immunofluorescence (IF ... biotechnology or pharmaceutical industry. * Experience supporting biomarker development or ...

System One

Scientist II

Ridgefield, CT · On-site

$35 - $40.05/hr

Perform quantitative analysis of histology, immunohistochemistry (IHC), immunofluorescence (IF ... biotechnology or pharmaceutical industry. * Experience supporting biomarker development or ...

System One

Scientist II

Ridgefield, CT · On-site

$35 - $40.05/hr

Perform quantitative analysis of histology, immunohistochemistry (IHC), immunofluorescence (IF ... biotechnology or pharmaceutical industry. * Experience supporting biomarker development or ...

previous pagenext page

Showing results 21-40

All JobsAnalytical Development Biotech JobsAnalytical Development Biotech Jobs in Connecticut

Analytical Development Biotech information

What are some typical challenges faced by analytical development professionals in the biotech industry?

Analytical Development professionals in biotech often encounter challenges such as developing robust methods for novel biologics, ensuring regulatory compliance, and adapting to rapid technological changes. They frequently work within cross-functional teams, collaborating closely with research, manufacturing, and quality assurance groups to optimize assay performance and troubleshoot issues. Staying current with evolving regulatory standards and balancing project timelines with method validation requirements are also common aspects of the role.

What is analytical development in the pharmaceutical industry?

Analytical development in the pharmaceutical industry involves creating and validating methods to accurately measure the quality, purity, and potency of drug substances and products. For an Analytical Development Biotech, this includes designing assays, optimizing analytical techniques like HPLC or mass spectrometry, and ensuring compliance with regulatory standards such as GMP and ICH guidelines.

What is the difference between Analytical Development Biotech vs Quality Control Analyst?

AspectAnalytical Development BiotechQuality Control Analyst
CredentialsBachelor's/Master's in Life Sciences, Chemistry, or related fieldsBachelor's in Chemistry, Biology, or related fields; often requires GMP training
Work EnvironmentResearch labs, development departments, collaborative teamsQuality labs, manufacturing facilities, compliance-focused settings
Industry UsageDeveloping and optimizing analytical methods for biotech productsTesting and ensuring product quality and compliance with standards

Analytical Development Biotech focuses on creating and refining analytical methods during product development, while Quality Control Analysts primarily test products to ensure they meet quality standards. Both roles require similar educational backgrounds and work in laboratory settings, but their core responsibilities differ in the product lifecycle.

What is analytical development in biotech?

Analytical Development in biotech refers to the process of designing, developing, and validating methods to analyze biological products, such as proteins, antibodies, or cell therapies, during various stages of drug development and manufacturing. These methods are essential for ensuring the safety, quality, potency, and purity of biotechnological products. Professionals in this field work closely with research, production, and regulatory teams to ensure that analytical methods meet industry standards and comply with regulatory requirements. Analytical Development is a critical part of bringing new biopharmaceutical products from the lab to the market.

What are the key skills and qualifications needed to thrive as an analytical development biotech professional?

To thrive as an Analytical Development Biotech professional, you need a strong background in analytical chemistry, biochemistry, or a related field, typically supported by at least a bachelor's or master's degree. Familiarity with analytical instrumentation such as HPLC, GC, mass spectrometry, and relevant quality systems like GMP or ICH guidelines is crucial. Strong problem-solving, attention to detail, and effective communication are important soft skills for collaborating across multidisciplinary teams. These competencies ensure accurate data generation, regulatory compliance, and successful development of biotechnological products.
What are popular job titles related to Analytical Development Biotech jobs in Connecticut? For Analytical Development Biotech jobs in Connecticut, the most frequently searched job titles are:
What job categories do people searching Analytical Development Biotech jobs in Connecticut look for? The top searched job categories for Analytical Development Biotech jobs in Connecticut are:
What cities in Connecticut are hiring for Analytical Development Biotech jobs? Cities in Connecticut with the most Analytical Development Biotech job openings:
Analytical Development Biotech jobs near you
Infographic showing various Analytical Development Biotech job openings in Connecticut as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

Executive Medical Director, Neurology, Clinical Development (Remote)

Penfield Search Partners

Fairfield, CT • On-site, Remote

Full-time

Posted 22 days ago

Job description

Contact: Alexandra Spink -
No 3rd party candidates

We are looking for an accomplished Executive Medical Director, Neurology Clinical Development to lead the strategy, execution, and oversight of global clinical development programs across neurology indications. This highly visible leadership role will drive clinical programs from early development through registration, provide medical leadership across cross-functional teams, and help shape the future of our neurology gene therapy portfolio.

As the medical lead for assigned programs, you will provide expert oversight of medical monitoring, clinical strategy, data interpretation, regulatory interactions, and scientific communications. Working collaboratively across Research, Clinical Operations, Regulatory Affairs, Biostatistics, Pharmacovigilance, Commercial, and other key stakeholders, you will play a critical role in advancing innovative therapies for patients with neurologic diseases.

Key Responsibilities

  • Lead the strategy, design, and execution of global clinical development programs across Phases I–III.
  • Serve as the therapeutic area lead for the Neurology Gene Therapy Clinical Development team, partnering with Clinical Operations, Toxicology, Regulatory Affairs, Commercial, Pharmacovigilance, Clinical Quality, and Biostatistics.
  • Provide medical oversight for clinical trials, ensuring patient safety, protocol compliance, data integrity, and study quality.
  • Lead clinical operational strategy, including site selection, enrollment, feasibility, and issue resolution.
  • Collaborate with Clinical Operations on medical monitoring, safety review, coding, and data cleaning.
  • Interpret clinical trial data and ensure the scientific integrity of study reports and communications.
  • Author or oversee clinical sections of regulatory submissions, including INDs, NDAs, BLAs, and briefing books.
  • Represent the company during regulatory agency interactions and Advisory Committee meetings.
  • Develop safety management documents, DMC charters, investigator communications, and other study-related materials.
  • Build relationships with CROs, investigators, key opinion leaders, consultants, and investigational sites.
  • Analyze and present clinical data through publications, presentations, scientific meetings, and advisory boards.
  • Maintain expertise in neurology and gene therapy through scientific literature and medical conferences.
  • Manage clinical development budgets, timelines, risks, and program progress.
  • Support business development, product evaluations, due diligence, and portfolio strategy.
  • Provide medical expertise to internal and external stakeholders across research, development, commercial, regulatory, manufacturing, and patient-focused functions.
  • Coach, mentor, and develop direct reports while fostering a collaborative, high-performing team.

Qualifications

  • MD (or foreign equivalent) with clinical training and experience in Neurology required.
  • PhD in a related scientific discipline preferred.
  • 10+ years of global clinical development experience in the pharmaceutical or biotechnology industry across Phases I–III.
  • 5+ years of leadership experience managing clinical development teams.
  • Pediatric neurology experience preferred.
  • Gene therapy experience preferred.
  • Strong expertise in medical monitoring, clinical trial design, regulatory strategy, and clinical data interpretation.
  • Thorough knowledge of ICH-GCP guidelines, FDA regulations, and global clinical development requirements.
  • Excellent leadership, communication, and cross-functional collaboration skills.
  • Ability to travel domestically and internationally up to 20%.