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Home-Based Position Full-time Telecommute Senior Medical Writer
Eingestellt von Real Staffing Group aus Frankfurt am Main
Gesuchte Skills: Client
Projektbeschreibung
Exciting CRO is growing by leaps and bounds - we are seeking highly experienced regulatory medical writers to work from home with occasional travel to the northeast office in New Jersey. Salary is extremely attractive at up to $115k/year - full benefits - excellent 401k match along with benefits!
This company has an excellent culture with easy access to upper level management - high visability and amazing career growth - the expansion this year is substantial and we truly are looking to build up this group to be one of the strongest groups in medical writing!
Responsibilities:
- Write CSRs, protocols, IBs, CSSs, CSEs, NDAs and INDs
- Work with inter-disciplinary teams especially regulatory affairs to facilitate submission strategies and fulfill client deliverables
- Work within set timelines and write independently on regulatory documents
- Provide advice and sit on meeting roundtables to discuss submission strategy and how writing will fit in
- Work with team members to produce high-quality documents
Requirements:
- At least 5 years of solid regulatory medical writing experience
- CRO and/or large pharmaceutical experience is required
- Pleasant personality with excellent communication skills
So far, I've made multiple placements with this same company - we are looking to continue building out this excellent group with strong medical writers - excellent work-life balance and culture!
Send your resume today to: Dandan Zhu at Real Pharma 212-707-8499To find out more about Real Staffing please visit www.realstaffing.com
This company has an excellent culture with easy access to upper level management - high visability and amazing career growth - the expansion this year is substantial and we truly are looking to build up this group to be one of the strongest groups in medical writing!
Responsibilities:
- Write CSRs, protocols, IBs, CSSs, CSEs, NDAs and INDs
- Work with inter-disciplinary teams especially regulatory affairs to facilitate submission strategies and fulfill client deliverables
- Work within set timelines and write independently on regulatory documents
- Provide advice and sit on meeting roundtables to discuss submission strategy and how writing will fit in
- Work with team members to produce high-quality documents
Requirements:
- At least 5 years of solid regulatory medical writing experience
- CRO and/or large pharmaceutical experience is required
- Pleasant personality with excellent communication skills
So far, I've made multiple placements with this same company - we are looking to continue building out this excellent group with strong medical writers - excellent work-life balance and culture!
Send your resume today to: Dandan Zhu at Real Pharma 212-707-8499To find out more about Real Staffing please visit www.realstaffing.com
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung