
Client Relationship Associate
5 days ago
**Requirements**:
- Minimum Qualifications: Bachelor's or advanced degree in Science (Compulsory)
- Preferred Educational Background: B. Pharma, BSC, M. Pharma.
- Experience performing literature searches and writing activities such as writing technical sections of regulatory documents, clinical reports, poster presentations, and manuscripts for publication in scientific journals.
- Attention to factual detail and accuracy and the ability to see relationships between ideas to organize complex information.
- Excellent written, editorial, oral, and presentation skills.
- Excellent verbal communication skills (Professional English)
- Experience with Microsoft Office, including presentation development in PowerPoint, and citation management program(s) such as Endnote.
- Knowledge and experience with medical terminology preferred.
- Familiarity with various clinical research activities and best practices including research study design, protocol development, data analysis, and regulatory requirements.
**Responsibilities**:
- Work in a collaborative team to develop conference materials (abstracts, posters, presentations), and peer-reviewed publications.
- Write, review, and edit scientific abstracts, manuscripts, clinical study reports, plan outlines, investigator brochures, posters, newsletters, book chapters, articles, documents, publications, and presentations.
- Coordinate with various authors, contributors, editors, and researchers to develop an understanding of timelines, tasks, priorities, schedules, and deadlines.
- Planning, conducting, and reporting literature searches (systematic and non-systematic), screening of abstracts and articles, data extraction, and quality assessment.
- Interpret non-clinical and clinical data in preparing reports and manuscripts for publication in peer-reviewed journals.
- Familiarity with the various critical appraisal tools used for different types of studies/publications.
- Ensure documents are formatted according to submission specifications.
- Work with authors to fact-check; clarify text; and prepare figures, tables, charts, legends, slides, and posters.
- Attend meetings, participate in committees, and obtain training related to research projects and medical writing.
- Maintain familiarity with industry practices and regulatory requirements that affect medical writing and publication.
- May assist in developing and designing graphics or other communication materials for various target audiences.
- May assist faculty, and research manager in protocol development.
- May review and edit analysis plans prepared by statisticians.
- May serve as a functional representative on assigned project teams.
- Work with departmental and divisional leadership to set goals, initiate and implement scientific and grant writing training for faculty, residents, and staff.
Schedule:
- Day shift
- Morning shift
**Education**:
- Master's (preferred)
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