Summary:
Do you love science? Do you like to write about science? Medical Writing (MW) might be a good choice for you. MW is a critical component of the drug development process. The MW is an integral part of the team crafting the story of a drug’s development, from both the nonclinical and clinical aspects. This may involve working on multiple types of documents from writing protocols to summarizing the results from early stages of testing in healthy volunteers all the way to Phase 3 efficacy and safety trials in patients.
MW is a team-oriented function that partners closely with various departments to craft the best possible documents, within Regulatory guardrails.
Scope:
- Performs necessary daily responsibilities in accordance with current Standard Operating Procedures (SOPs).
- Manage MW timelines for individual projects with supervisor and project team input. Recognizes potential scheduling and resource conflicts for writing projects and provides recommendations to resolve.
- Communicates with team members regarding deliverables, document timelines, and processes.
- Supports the lead MW with interpretation of data generated from a variety of sources. Assists with drafting text, as appropriate.
- Verifies completeness and accuracy of the writing.
- Supports the coordination of review and approval of clinical and regulatory documents. Attends and assists in review meetings with the team.
- Supports the maintenance of medical writing systems, SOPs, work instructions, and standardization tools.
- Supports ad hoc and miscellaneous job-related projects, as assigned. Accepts new responsibilities, as needed.
Education/Experience/Qualifications:
- Must be currently enrolled in a 4-year bachelor program, preferably a Life Science or Biological Science major in their Junior or Senior year.
- Grade point average of 3.5 or above.
- Must be a self-starter, have strong communication skills, interpersonal skills, as well as strong attention to detail.
- Must have good verbal and written communication skills.
- Must be proficient with computers/software (Word, Excel, PowerPoint).
- This is a part-time (up to 20 hours/week) assignment for a duration of 6-12 months.
- This is a hybrid role to where you will be required to be onsite 4 hours/week in our San Diego office.
Gossamer Bio is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants and complies with all applicable national, state and local laws governing nondiscrimination in employment.The expected salary range for this position is $20 to $25/hr. Actual pay will be determined based on experience, qualifications, and other job-related factors permitted by law.
Vaccination Policy:
Gossamer Bio is committed to complying with federal, state and local law on vaccinations. Job candidates and employees should be aware that some roles may require full vaccination against COVID-19 . Gossamer Bio is an equal opportunity employer, and will provide reasonable accommodation to those unable to be vaccinated where it is not an undue hardship to the company to do so as provided under federal, state, and local law.
California Consumer Privacy Act (CCPA) Notice for California Residents:
This notice is to notify you that personal data about you has been collected by Gossamer Bio (“Controller”), which is located at 3115 Merryfield Row, Suite 120, San Diego CA 92121 and can be contacted by emailing privacy@gossamerbio.com, because Controller wishes to evaluate your candidacy for employment at Controller.Your personal data was either obtained from publicly available sources (e.g. LinkedIn) or provided to Controller by someone who referred you for potential employment. Controller’s Privacy team can be contacted at privacy@gossamerbio.com.
Your personal data will be processed for the purposes of managing Controller’s recruitment related activities, which include setting up and conducting interviews and tests for applicants, evaluating and assessing the results thereto, and as is otherwise needed in the recruitment and hiring processes. Such processing is legally permissible under Art. 6(1)(f) of Regulation (EU) 2016/679 (General Data Protection Regulation) and the California Consumer Privacy Act (CCPA) as necessary for the purposes of the legitimate interests pursued by the Controller, which are the solicitation, evaluation, and selection of applicants for employment.Your personal data has been shared with Greenhouse Software, Inc., a cloud services provider located in the United States of America and engaged by Controller to help manage its recruitment and hiring process on Controller’s behalf.
Your personal data will be retained by Controller as long as Controller determines it is necessary to evaluate your application for employment. Under the GDPR and CCPA, you have the right to request access to your personal data, to request that your personal data be rectified or erased, and to request that processing of your personal data be restricted. You also have to right to data portability. In addition, you may lodge a complaint with a supervisory authority.
