A research organization has an open position for a Telecommute TechnicalWriter V. Must be able to: Develop documents in accordance with Company standards and templates. Draft process maps to illustrate process flow as it relates to the procedures.
Collaborating with the Medical Writer on clinical regulatory documents. Must meet the following requirements for consideration: 20-30% travel required. BS with 7+ years’; or MS with 5+ years’; or PhD with <2 years’ relevant career experience. Oncology experience required.
Core Responsibilities of this position include: Producing technical documentation and accompanying exploit code. Working alongside senior research team members. Applicants must meet the following qualifications: Demonstrated understanding of common vulnerability classes.
Overseeing the development of competitive intelligence, training, and technical/sales enablement tools. Managing primary and third party research efforts to strengthen business resilience frameworks. Must meet the following requirements for consideration:
At least 15 years of progressively senior technical IT security, identity and architecture experience. Excellent writing and research skills coupled with strong analytical skills. Broad knowledge of IAM industry trends and emerging technologies.
Helping to establish and build high-level relationships. Providing specialized technical support. Applicants must meet the following qualifications: 25% travel required. Solid understanding of medical laboratories. Bachelor's Degree and minimum 4 years of relevant experience.
A staffing agency has an open position for a Remote Principal BioPharma Medical Writer. Candidates will be responsible for the following: Leading the composition of all clinical and regulatory deliverables. Reviewing all regulatory/clinical documents composed by outside sources.
Core Responsibilities Include: Driving efficient and high quality technical data delivery. Evaluating and managing project milestones. Supporting data delivery and technical solutions initiatives. Must meet the following requirements for consideration:
Ability to travel as needed. Bachelor’s Degree in a Scientific or Technical Discipline. 15+ years experience with expert level industry/regulatory knowledge. Experience in Small Molecule CMC. Previous experience with a regulatory agency (such as FDA, MHRA)
Ability to represent company at client marketing and technical meetings. PhD in related field with 4 years experience or Master's and 6 years experience. Comprehensive knowledge of statistical theory. Expertise in SAS programming. Experience in all tasks of a Trial Statistician.