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Associate Medical Writer Jobs in Connecticut (NOW HIRING)

Collabera

Technical Writer

North Haven, CT · On-site

... days, Medical, Dental and Vision insurance, 401K retirement savings plan, Life Insurance ... Associates degree in Technical Communications or related field, bachelor's degree preferred.

RVNAhealth

Grant Writer - Part Time

Ridgefield, CT

$34 - $36/hr

Work with the Development Associate to maintain accurate grant and donor records within the donor ... medical conditions, national origin, age, physical and mental disability, marital status, sexual ...

RVNAhealth

Grant Writer - Part Time

Ridgefield, CT · On-site

$34 - $36/hr

Work with the Development Associate to maintain accurate grant and donor records within the donor ... medical conditions, national origin, age, physical and mental disability, marital status, sexual ...

FuelCell Energy

Senior Technical Writer

Danbury, CT · On-site

$65K - $80K/yr

Associate degree or higher in engineering, technology, technical communication, English, or a ... We offer a competitive compensation package as well as comprehensive benefits including medical ...

FuelCell Energy

Senior Technical Writer

Danbury, CT · On-site

$65K - $80K/yr

Associate degree or higher in engineering, technology, technical communication, English, or a ... We offer a competitive compensation package as well as comprehensive benefits including medical ...

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All JobsAssociate Medical Writer JobsAssociate Medical Writer Jobs in Connecticut

Associate Medical Writer information

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$13

$36

$55

How much do associate medical writer jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for associate medical writer in Connecticut is $36.75, according to ZipRecruiter salary data. Most workers in this role earn between $24.90 and $46.44 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an associate medical writer?

To thrive as an Associate Medical Writer, you need a solid background in life sciences, strong writing abilities, and attention to detail, often supported by a relevant degree such as biology, pharmacy, or medicine. Familiarity with referencing tools (e.g., EndNote), medical literature databases (e.g., PubMed), and proficiency in Microsoft Office are typically required. Excellent communication, time management, and the ability to interpret complex scientific data set standout candidates apart. These skills ensure that scientific information is accurately and clearly communicated to varied audiences, supporting effective healthcare and regulatory decision-making.

What are some common challenges faced by associate medical writers during their first year on the job?

In their first year, Associate Medical Writers often find it challenging to quickly adapt to diverse writing styles and strict formatting guidelines required by different clients or regulatory bodies. Balancing tight deadlines while ensuring scientific accuracy and compliance can also be demanding, especially when juggling multiple projects. Additionally, learning to effectively collaborate with multidisciplinary teams—including clinicians, researchers, and senior writers—requires strong communication and organizational skills. However, with mentorship and constructive feedback, these challenges become valuable learning opportunities for professional growth.

What is the difference between Associate Medical Writer vs Medical Writer?

AspectAssociate Medical WriterMedical Writer
Required credentialsBachelor's degree, often in life sciences or related fieldBachelor's or higher degree, often with some experience
Work environmentEntry-level, training-focused, often in pharmaceutical or biotech companiesMore independent, involved in complex document creation for regulatory or scientific purposes
Employer usagePharmaceutical, biotech, medical communications agenciesPharmaceutical companies, CROs, medical communication firms

The main difference between an Associate Medical Writer and a Medical Writer lies in experience and responsibility. Associate Medical Writers are typically entry-level, focusing on learning and supporting document preparation, while Medical Writers handle more complex projects independently. Both roles require similar educational backgrounds and are common in the pharmaceutical and biotech industries.

What does an associate medical writer do?

An Associate Medical Writer is responsible for creating scientific documents, such as clinical study reports, regulatory submissions, and manuscripts for publication. They work closely with medical professionals, researchers, and regulatory teams to ensure accuracy and compliance with guidelines. Their role often involves interpreting complex scientific data and presenting it in a clear, concise manner for different audiences. Associate Medical Writers are typically early in their medical writing careers and receive guidance from more senior writers as they develop their skills.
What are the most commonly searched types of Medical Writer jobs in Connecticut? The most popular types of Medical Writer jobs in Connecticut are:
What are popular job titles related to Associate Medical Writer jobs in Connecticut? For Associate Medical Writer jobs in Connecticut, the most frequently searched job titles are:
What job categories do people searching Associate Medical Writer jobs in Connecticut look for? The top searched job categories for Associate Medical Writer jobs in Connecticut are:
What cities in Connecticut are hiring for Associate Medical Writer jobs? Cities in Connecticut with the most Associate Medical Writer job openings:
Associate Medical Writer jobs near you
Infographic showing various Associate Medical Writer job openings in Connecticut as of August 2026, with employment types broken down into 75% Full Time, 16% Part Time, 2% Temporary, and 7% Contract. Highlights an 79% In-person, 8% Hybrid, and 13% Remote job distribution, with an average salary of $76,449 per year, or $36.8 per hour.

Associate Director, Medical Writer

Celldex Therapeutics, Inc.

New Haven, CT • On-site

$153.62 - $199.50/hr

Other

Medical, Retirement, PTO

Re-posted 17 days ago

Job description

Overview

The Associate Director, Medical Writer at Celldex will lead the development and management of complex clinical and regulatory documents, including protocols, investigator brochures, study reports, and regulatory submissions for our immunology programs. This role requires extensive medical writing expertise, cross-functional project leadership, and the ability to drive timelines and ensure compliance with regulatory standards in a fast-paced clinical development environment.

Responsibilities
  • Responsible for the generation of clinical regulatory documents including, but not limited to: briefing documents, IND annual reports, Investigator's Brochures, clinical protocols and amendments, clinical study reports, scientific manuscripts and abstracts.
  • Assume a lead role in creation, execution and monitoring of complex documents, project plans, management of timelines, and coordination of review meetings. Plan and coordinate timely review, revision and approval of clinical documents.
  • Research and ensure compliance with applicable regulatory guidance, style guidelines and departmental SOPs; remain abreast of professional information and technology.
  • Contribute to process improvements related to creation and maintenance of clinical documentation.
  • Assist other departments with writing projects on an ad‑hoc basis.
  • Partial remote work can be accommodated. Must be able to work on‑site, attend business meetings, and travel between Celldex’s locations and for business as required.
Qualifications
  • Completed BA/BS degree is required, with a concentration in a scientific or health care field preferred.
  • Must have 5-10 or more years of experience as a medical writer preparing clinical regulatory submission documents.
  • Experience in medical writing project leadership roles for complex submissions, preferably within the field of immunology.
  • Later phase writing experience (e.g., Phase 3) and BLA/NDA experience in immunology are strongly preferred.
  • Demonstrated ability to meet project goals within a matrix environment. Lead document writing and related work for clinical development projects.
  • Strong analytical mind, excellent written/verbal communication skills, attention to detail, organizational skills, and ability to work independently and as part of a team.
  • Strong document management skills, including proficiency with MS Word, EndNote, and Excel.
Compensation

The expected base salary range for this position is $153,616 to $199,501.

We are committed to compensating employees equitably based on several factors including experience, education, licensure/certifications, skill level, location of the position, and availability of similar talent in a competitive market.

Compensation for this role includes base salary, annual discretionary bonus, long term incentive, 401(K) plan with employer contribution, health care and other insurance benefits (for employee and family), paid holidays, vacation, and sick days. A summary of our benefits can be found on our careers page.

Celldex is proud to be an equal opportunity employer that strives to foster a culture of diversity, equity, and inclusion. We are committed to promoting a diverse environment through development, recruiting and community outreach.

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