Filters:
State: Georgia
Show
|
Clear
1
22 Results
Resume Writing & Professional Services
Our professional resume writing service has helped over 1 million professionals land more interviews and get hired faster.
AD
Preferred Diversity Focus
EyePoint Pharmaceuticals
Watertown, Massachusetts, United States (remote)
5 days ago
Preferred Diversity Focus
EyePoint Pharmaceuticals
Remote, United States (remote)
21 days ago
Preferred
NIH National Institute on Aging
Bethesda, Maryland, United States (remote)
30+ days ago
X4 Pharmaceuticals
Massachusetts, United States (remote)
7 days ago
X4 Pharmaceuticals
Illinois, United States (remote)
7 days ago
stratacuity
Boston, Massachusetts, United States (remote)
12 days ago
stratacuity
Cambridge, Massachusetts, United States (remote)
12 days ago
Sarepta Therapeutics
Massachusetts, United States (remote)
17 days ago
Sarepta Therapeutics
Massachusetts, United States (remote)
17 days ago
Sarepta Therapeutics
Massachusetts, United States (remote)
17 days ago
Sarepta Therapeutics
Massachusetts, United States (remote)
17 days ago
Sarepta Therapeutics
Massachusetts, United States (remote)
17 days ago
Sarepta Therapeutics
Massachusetts, United States (remote)
17 days ago
stratacuity
Massachusetts, United States (remote)
26 days ago
MorphoSys
Boston, Massachusetts, United States (remote)
27 days ago
T1D Exchange
Boston, Massachusetts, United States (remote)
28 days ago
T1D Exchange
Boston, Massachusetts, United States (remote)
28 days ago
ONTOFORCE
30+ days ago
Stealth BioTherapeutics
Massachusetts, United States (remote)
30+ days ago
Celldex Therapeutics Inc
United States (remote)
30+ days ago
Sarepta Therapeutics
Cambridge, Massachusetts, United States (remote)
30+ days ago
1 - 22 Results of 22
EyePoint Pharmaceuticals
Watertown, Massachusetts, United States
(remote)
Preferred Diversity Focus Member Company
5 days ago
Job Type
Full-Time
Job Duration
Indefinite
Min Experience
7-10 Years
Min Education
BA/BS/Undergraduate
Required Travel
0-10%
Work Setting
Non-Lab
Job Function

Description

Senior Director/Director, Medical Writer
Job LocationsUS-MA-Watertown | US
Job ID2024-1375

Overview

Be Seen and Heard at EyePoint Pharmaceuticals

At EyePoint, leadership trusts our employees to get the job done. The patient-centric and award-winning approach we’re taking in business fuels our success for:

  • preventing blindness through vision-saving medications
  • delivering best-in-class proprietary pharmaceutical technologies
  • transforming ocular drug delivery

We See You.

Your wellbeing

Your professional worth

Your future at EyePoint

EyePoint offers robust total rewards in a science-based entrepreneurial culture that empowers curiosity and innovation to help catapult your career. There’s space for every voice and perspective to be heard in our on-site and remote environments where a variety of strengths and diverse backgrounds are connected.

We are seeking a Sr. Director/Director level Medical Writer to manage Clinical deliverables.This person will report into the VP, Clinical Development. We offer a competitive salary, bonus structure and stock. For local candidates near our Watertown, MA site, we offer a hybrid work schedule (on-site 2-3 days a week), or this person can work fully remote if not local.

The salary range depends on the level of the position: $220 base salary up to $270 range. 

This person should have a positive attitude and be adaptable to a dynamic startup environment.

Responsibilities

Primary responsibilities include, but are not limited to, the following:

Individual responsibilities

  • Provides Medical Writing leadership for all assets from pre-IND to NDA.
  • Acts as a medical writing subject matter expert and works with clinical and regulatory team to deliver on medical writing program goals.
  • Oversees and contributes directly to the development of a variety of clinical documents for clinical and regulatory purposes, including clinical protocols, clinical study reports, investigator brochures, IND and NDA and other regulatory submissions documents. Must be attentive to details within documents.
  • Oversee, and contribute directly to, the development of summarizing the emerging clinical data.
  • Coordinate the efforts of cross-functional teams to produce high-quality, scientifically accurate documents.
  • Oversees and contributes directly to the planning, process and coordination timelines to ensure timely completion of clinical writing projects.
  • Manage timelines and communicate with team stake holders to maintain awareness of expectations, milestones, and deliverables.
  • Provide support for QC of complex clinical documents.
  • Ensure that the key messages in protocols, clinical documents, and regulatory documents align with each other, and also with the Investor Relations documents.
  • Possesses a roll-up-your sleeves attitude; may work with other external contributors and is self-directed. 


Requirements

Qualifications

Primary skills and knowledge required include, but are not limited to the following:

  • A depth of experience in clinical-regulatory writing (Protocols, IBs, CSRs, Module 2 experience and briefing books) for pharmaceutical companies
  • Experience working with vendors, and consultants.
  • Cross functional team player
  • Self-motivated, attention-to-detail, excellent interpersonal-organizational and time management skills

Other Requirements:

They must have a positive attitude and be adaptable to a dynamic “startup” type of environment.  This individual should be a strong and dependable team member who builds trust with management.  They must be transparent, ethical, and honest, and foster a culture of the same within their team. 

Level of Education Required:

Bachelor’s degree

Number of Years of Experience in the Function and in the Industry:

  • 10+ years’ experience working as a Medical Writer in a pharmaceutical or Biotechnology industry.
  • Ophthalmology experience is highly preferred.

Envision Your Future

With the exciting energy of a winning culture and an exhilarating pace, we are an ophthalmology company committed to preventing blindness by developing and commercializing innovative therapeutics.

The collective power of our values influences everything we do, and everything we do for you.

  • Success begins with our People
  • Patients First
  • Integrity
  • Results-Driven
  • Innovation
  • Team Focus
  • Diversity & Inclusion

EyePoint Pharmaceuticals is proud to be an equal opportunity employer. We believe that diversity and inclusion among our colleagues is critical to our success as a company, and we seek to recruit, develop, and retain the most talented people from a diverse candidate pool. All applicants will be considered for employment without attention to age, race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status.

#LI-Hybrid

#LI-Remote

Job ID: 72502141

See Your Future with EyePoint Pharmaceuticals We are proud to be named a winner of the 2021 Deloitte Technology Fast 500 award, which recognizes the most innovative, fastest-growing companies in North America. We’re challenging the status quo in bio tech with a singular focus on vision-saving medications delivered through best-in-class proprietary pharmaceutical technologies and unique internal manufacturing capabilities to transform ocular drug delivery. Our unique culture fosters a science-based entrepreneurial envi...

View Full Profile

View your connections
Jobs You May Like
Filters
Workplace Type
Job Function
Work Setting
Min Education
State