Entry level medical writer Jobs in Lynn, MA
Last updated: 13 hours ago
Senior Manager, Medical Writing.Seaport) - Hybrid (3 days onsite per week).Bachelor’s + 7 years, Master’s + 5 years, or PhD + 2 years of experience in medical writing or a related field.Experience ...Show moreLast updated: 6 days ago
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Synterex offers remote or on-site services, with a focus on providi...Show moreLast updated: 20 days ago
Growing NationalLaw Firm in Bostonhas a need for an AssociateAttorney.Can be entry level up to 4 years of legal experience.
This is a direct hire opening with a full benefits package.Active membersh...Show moreLast updated: 19 days ago
Licensed Life Insurance Agents.Life Insurance Agency partnered with Symmetry Financial Group.Our agents help families in their regional area or whatever territory they choose working remotely with ...Show moreLast updated: 30+ days ago
This role is for a skilled Medical Writer to create and refine essential documents for clinical studies and regulatory submissions on a part-time basis.
Lead and write clinical documents like protoc...Show moreLast updated: 21 days ago
FREE movies tickets & flexible schedules!o Job descriptions are available in cinema or refer to.As a Showcase Cinemas employee, you are required to work during our peak business times (e.Show moreLast updated: 1 day ago
MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, including clinical trial transparency, and medical device industries with a proven, scientific approach to com...Show moreLast updated: 30+ days ago
The Principal Medical Writer represents medical writing on multi-disciplinary teams, collaborates on the development of clinical documents in accordance with all applicable regulations, Good Clinic...Show moreLast updated: 10 days ago
Location : Cambridge, MA (Hybrid)Science / Focus : .This role is for a skilled Medical Writer to create and refine essential documents for clinical studies and regulatory submissions on a part-time ba...Show moreLast updated: 1 day ago
Location : Cambridge, MA (Hybrid)Science / Focus : .This role is for a skilled Medical Writer to create and refine essential documents for clinical studies and regulatory submissions on a part-time ba...Show moreLast updated: 1 day ago
As a medical writer for Aquent Studios, you will be responsible for writing documents, articles, journals, brochures, and product manuals for our pharma clients’ organizations.You will cover topics...Show moreLast updated: 30+ days ago
Role SummaryResponsibilities : You will work on projects that involve the detailed analysis and presentation of clinical data, which are instrumental to the successful uptake of novel therapiesSalar...Show moreLast updated: 13 hours ago
Our client, a Global Investment Bank, is seeking an Entry Level Analyst in Boston, MA : .Assist in preparing financial reports and statements, including monthly, quarterly, and annual reports.Conduct...Show moreLast updated: 21 days ago
Sorry, Visa / sponsorship not available.Salary - $50k to $60k - depending on experience.Dental insurance, Health insurance, Life insurance, Paid time off, Vision insurance.Must have 1 plus years' c...Show moreLast updated: 30+ days ago
This role is for a skilled Medical Writer to create and refine essential documents for clinical studies and regulatory submissions on a part-time basis.
Lead and write clinical documents like protoc...Show moreLast updated: 15 hours ago
- Promoted
Sr Manager, Medical Writer
Planet PharmaBoston, MA, United States$87.00 hourly
Full-time
- Promoted
Senior Medical Writer (Contract)
SynterexBoston, Massachusetts, USFull-time
- Promoted
Attorney - Entry Level
Kosmos CorpBoston, Texas, USAPermanent
- Promoted
Entry Level Sales
The WRS Group - Symmetry FinancialBoston, MA, USFull-time
- Promoted
Medical Writer 2057623
Stratacuity : Proven Scientific PlacementCambridge, MA, United StatesPart-time
- Promoted
Entry Level Bartender
Showcase Cinemas - Chestnut HillEverett, MA, USFull-time
Principal Medical Writer
MMSBoston, MA, USQuick Apply
- Promoted
Principal Medical Writer
Alnylam PharmaceuticalsCambridge, MA, United StatesFull-time
Medical Writer
MediabistroCambridge, MA, United StatesPart-time
Medical Writer
StratacuityCambridge, MA, United StatesPart-time
Medical / Scientific Writer
Vitamin TBoston, MA$70.00–$75.00 hourly
- New!
Analyst / Medical Writer
Costello MedicalBoston, MA, United States$73,000.00 yearly
Permanent
- Promoted
Entry Level Analyst
Phyton Talent AdvisorsBoston, MA, United StatesFull-time
Senior Medical Writer
Advanced ClinicalCambridge, MA, US We are currently searching for a skilled professional to join a well-known client’s team as a Sr.Medical Writer in Watertown, MA working onsite 2-3 days a week, with some flexibility.Medical Writer...Show moreLast updated: 30+ days ago
- Promoted
Customs Entry Writer
FreightTAS LLCBoston, MAFull-time
- New!
Medical Writer
Apex SystemsCambridge, MAPart-time
Quick Apply
- Promoted
Medical Assistant - Entry Level Training Program
Dreambound Inc.Boston, Massachusetts This is an educational program, not a job offer.Successful completion of the program does not guarantee employment but will equip you with valuable skills for the healthcare job market.Looking to s...Show moreLast updated: 30+ days ago
Sr Manager, Medical Writer
Planet PharmaBoston, MA, United States6 days ago
Salary
$87.00 hourly
Job type
- Full-time
Job descriptionDocument Development : Independently author and manage the development of clinical and regulatory documents, including protocols, clinical study reports, investigator brochures, safety reports, briefing documents, clinical summaries, publications, and regulatory submissions. Vendor Oversight : Initially, a significant portion of the role will involve managing external vendors for document preparation. Over time, smaller projects will be brought in-house, and you’ll oversee consultants and external writing resources. Collaboration : Work closely with cross-functional teams, including clinical, regulatory, and subject matter experts, to gather data, provide strategic input, and ensure that documents are clear, concise, and compliant with regulatory guidelines. Project Management : Develop and maintain timelines for document delivery, ensuring deadlines are met and quality standards are upheld. Manage competing priorities and communicate progress and issues to senior management. Regulatory Expertise : Ensure all documents comply with global regulatory guidance (e.g., ICH, FDA, EMA) and support the clinical development process at various stages. Process Improvement : Identify areas for process optimization and recommend improvements in document development or vendor management practices. Bachelor’s + 7 years, Master’s + 5 years, or PhD + 2 years of experience in medical writing or a related field. Proven experience in writing and managing regulatory and clinical documents in the pharmaceutical or biotech industry. Experience with pulmonary fibrosis is a must; oncology experience is highly preferred. Strong organizational, project management, and communication skills. Ability to work effectively under pressure and manage multiple priorities. Proficiency in global regulatory guidelines (FDA, EMA, ICH). Experience working with external vendors and consultants. Ability to interpret clinical data and summarize it in clear, concise text for regulatory submissions. Familiarity with publicly available databases (e.g., PubMed, FDA, EMA) for literature and information mining. This position is a hybrid role, requiring 3 days per week onsite in our Seaport, Boston office. The interview process will involve an initial meeting with the team followed by onsite interviews with the team. Parking : The company offers a $175 / month commuter subsidy for parking. The attached garage costs approximately $87 per paycheck, with a nearby lot available for $110 per paycheck.
Senior Manager, Medical Writing
Location : Boston, MA. (Seaport) - Hybrid (3 days onsite per week)
Base Salary : $170,000 - $200,000
Bonus : 18%
Equity : 55,000
Commuter Subsidy : $175 / month (Parking)
Estimated Start Date : Late February.
Education : Bachelor’s + 7 years, Master’s + 5 years, or PhD + 2 years of experience in medical writing or a related field.
Top 3 Skills :
- Experience with Pulmonary Fibrosis or LYT-100 is required
- Strong knowledge of global regulatory guidelines (FDA, EMA, ICH)
- Proven experience collaborating with external vendors and consultants
Role Overview
We are seeking a Senior Manager, Medical Writing to join the team supporting our pulmonary and oncology programs, specifically LYT-100 (pulmonary fibrosis) and LYT-200 (cancer). This role is pivotal in managing the writing and development of regulatory and clinical documents, as well as overseeing outsourced vendors. This is a hybrid position with 3 days per week onsite in our Boston office.
The Senior Manager will be the sole medical writer on the team and will report directly to Head of Clinical Development. The role offers an exciting opportunity to contribute to cutting-edge programs in the field of pulmonary fibrosis and oncology, with the flexibility to work alongside project teams and vendors to ensure timely, high-quality document production.
Key Responsibilities
Basic Qualifications
Education : Bachelor’s degree in a life sciences discipline (advanced degrees preferred).
Experience :
Skills :
Additional Information