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Drug Development Jobs in Wallingford, CT (NOW HIRING)

Labcorp

Phlebotomist - Float

New Britain, CT

Labcorp is a leader in diagnostics, drug development and healthcare innovation. Across every role, we harness data and AI to work smarter, move faster and create breakthrough solutions that improve ...

Labcorp

Phlebotomist - Float

New Britain, CT · On-site

$18 - $21.50/hr

Labcorp is a leader in diagnostics, drug development and healthcare innovation. Across every role, we harness data and AI to work smarter, move faster and create breakthrough solutions that improve ...

Labcorp

Medical Courier

New Britain, CT · On-site

$15.50 - $19.75/hr

Labcorp is a leader in diagnostics, drug development and healthcare innovation. Across every role, we harness data and AI to work smarter, move faster and create breakthrough solutions that improve ...

Source Medical, LLC.

Urology Physician

Hartford, CT

Access to a dedicated phase 1 research unit for early drug development Participation in weekly tumor boards and educational symposiums in collaboration with MSK Cancer Institute includes over 40 ...

Source Medical, LLC.

Urology Physician

Hartford, CT · On-site

Access to a dedicated phase 1 research unit for early drug development Participation in weekly tumor boards and educational symposiums in collaboration with MSK Cancer Institute includes over 40 ...

BAS Healthcare

Neuro-Oncologist Hartford

Hartford, CT · On-site

$201.75/hr

Participate in a phase 1 unit for early drug development studies * Engage system-wide in quality, research, and program development through established disease management teams and medical, radiation ...

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All JobsDrug Development JobsDrug Development Jobs in Wallingford, CT

Drug Development information

See Wallingford, CT salary details

$33.1K

$77.7K

$133.4K

How much do drug development jobs pay per year?

As of Aug 9, 2026, the average yearly pay for drug development in Wallingford, CT is $77,650.00, according to ZipRecruiter salary data. Most workers in this role earn between $58,700.00 and $90,700.00 per year, depending on experience, location, and employer.

What career develops drugs?

A career in drug development typically involves roles such as pharmacologist, medicinal chemist, clinical researcher, or regulatory affairs specialist. These professionals work in laboratories, research institutions, or pharmaceutical companies to discover, test, and bring new drugs to market, often requiring knowledge of biology, chemistry, and regulatory processes.

What is the difference between Drug Development vs Pharmacologist?

AspectDrug DevelopmentPharmacologist
Required CredentialsBachelor's or Master's in Pharmaceutical Sciences, Chemistry, or related fields; often requires experience in clinical trialsDegree in Pharmacology, Pharmacy, or related fields; may require licensing or certification for clinical practice
Work EnvironmentResearch labs, pharmaceutical companies, clinical trial sitesResearch labs, hospitals, academic institutions, regulatory agencies
Industry UsageDeveloping new drugs, overseeing clinical trials, regulatory submissionsStudying drug effects, mechanisms, safety, and efficacy; advising on drug use

While both roles are integral to the pharmaceutical industry, Drug Development focuses on creating and bringing new drugs to market through research, testing, and regulatory processes. Pharmacologists primarily study how drugs interact with biological systems, often working in research or clinical settings to understand drug effects and safety. The two roles often collaborate but differ in their core responsibilities and career focus.

What are the key skills and qualifications needed to thrive in drug development, and why are they important?

To thrive in Drug Development, you need a strong background in pharmaceutical sciences, biology, or chemistry, often supported by an advanced degree (e.g., PhD, PharmD, or MSc). Familiarity with regulatory compliance, clinical trial management systems, and data analysis software such as SAS or R is typically required. Excellent problem-solving, project management, and cross-functional communication skills help professionals excel in this multidisciplinary field. These competencies ensure that new drugs are developed safely, efficiently, and in accordance with regulatory standards.

What is drug development?

Drug development is the process of bringing a new pharmaceutical drug to market. It involves several stages, including drug discovery, preclinical research, clinical trials, and regulatory approval. Each stage is designed to ensure the safety, efficacy, and quality of the drug before it can be made available to patients. The entire process can take several years and requires collaboration between scientists, clinicians, regulatory agencies, and pharmaceutical companies.

How much do drug development professionals make?

Drug development professionals, including roles such as research scientists and clinical trial managers, typically earn between $70,000 and $130,000 annually, depending on experience, education, and location. Entry-level positions may start lower, while senior roles with advanced skills and certifications can exceed this range.

How do you get into drug development?

To enter drug development, individuals typically need a background in life sciences such as biology, chemistry, or pharmacology, often supported by a relevant bachelor's or advanced degree. Gaining experience through internships, research projects, or entry-level roles in pharmaceutical or biotech companies can be valuable, along with developing skills in laboratory techniques, data analysis, and regulatory compliance.

What are the typical stages of collaboration between different teams in a drug development role?

In drug development, professionals regularly collaborate across multidisciplinary teams, including research scientists, clinical trial coordinators, regulatory affairs specialists, and manufacturing experts. Early stages involve close work with research and discovery teams to identify promising compounds, followed by coordination with clinical teams during trial phases, and finally with regulatory and production teams as the drug moves toward approval and commercialization. Effective communication and cross-functional teamwork are essential, as each stage relies on timely data sharing and joint problem-solving to navigate complex challenges.
What job categories do people searching Drug Development jobs in Wallingford, CT look for? The top searched job categories for Drug Development jobs in Wallingford, CT are:
What cities near Wallingford, CT are hiring for Drug Development jobs? Cities near Wallingford, CT with the most Drug Development job openings:
Drug Development jobs near you
Infographic showing various Drug Development job openings in Wallingford, CT as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 17% Part Time, and 4% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $77,650 per year, or $37.3 per hour.

Associate Scientist II, Injectable Drug Product Development

Alexion Pharmaceuticals

New Haven, CT • On-site

Full-time

Posted 17 days ago

Job description

This is what you will do:

The Associate Scientist II candidate will be a part of the Injectable Drug Product Development (IDPD) team within the Pharmaceutical Development and Clinical Supply (PDCS) department at Alexion-AstraZeneca Rare Disease. The job entails experimental work on various aspects of drug product formulation and process development activities in support of drug product manufacturing, characterization, including analytical and biophysical comparability testing. The ability to work with minimal supervision as well as being part of a collaborative team is essential. The position entails study design, execution, and preparation of development reports and other required documentation.

You will be responsible for:

  • With some supervision, design and execute formulation and process development studies for clinical biologic candidates.
  • Execute drug development studies including physico-chemical characterization and stability studies for clinical and commercial drug products.
  • Characterize conformational and colloidal stability using industry standard methodology (e.g., circular dichroism, differential scanning fluorimetry, analytical ultracentrifugation, size-exclusion chromatography with multi-angle light scattering detection, etc.)
  • Maintain organized records and use team tools to keep multiple assignments on track.
  • Assist in the preparation of internal technical reports on executed studies with minimal supervision.
  • Participate in cross-functional development teams.

You will need to have:

  • BS or MS degree in Biochemistry, Pharmaceutical Science, Chemical Engineering, or relevant field with 2 to 4 years relevant work experience with a pharmaceutical or biotechnology company
  • Scientific and practical knowledge of protein/peptide biochemistry, protein formulation, and stability is essential.
  • Experience of working with imaged capillary electrophoresis (iCE/Maurice), H/UPLC's (IEX, SEC), DLS, CD, DSC, AUC, and NanoTemper
  • Ability to execute experiments with minimal supervision is required.
  • The individual must be able to work in a collaborative setting and has ability to adhere to timelines is essential.
  • Excellent interpersonal, collaborative and communication skills
  • Ability to take initiative in problem solving and finding solutions to scientific challenges.
  • Experience with various software packages like MS Office programs, including Word, Excel, Outlook, and PowerPoint
  • The duties of this role are generally conducted in a lab environment. As is typical of a lab-based role, employees must be able, with or without an accommodation to: lift/carry 15/30 pounds unassisted/assisted; work comfortably in a controlled environment with and around biological, infectious and hazardous materials; gown/degown PPE; use a computer; engage in communications via phone, video and electronic messaging; engage in problem solving and non-linear thought, analysis and dialogue; collaborate with others; maintain general availability during standard business hours.

We would prefer you to have:

  • Hands-on experience with process development, scale up, tech transfer, and manufacturing.
  • Experience working with sub-visible particle testing and characterization.
  • Experience of working with biophysical and analytical testing
  • Familiarity with regulatory guidelines.
  • High level proficiency in MS Office software including Word, Excel, Outlook, and PowerPoint.
  • Experience with electronic record keeping software, like ELN, EndNote, e-logbooks; maintenance of laboratory instrumentation (organizing PMs, data backup, SW upgrade, etc.) will be a plus.

Date Posted

23-Jul-2026

Closing Date

05-Aug-2026

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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