北京招聘

SUMMARY:

Performs data entry, creation and maintenance of files, spreadsheets, proposals, and reports. Assists with the reviews and analyses of project specific data and management of study-related committees.

ESSENTIAL FUNCTIONS:

1. Performs data entry of medical monitor contact reports (MMCRs) into ProjecTrend and/or IMPACT, while tracking and organizing MMCR data.

2. Assists Medical Affairs Scientists with review of medical data listings, Case Report Form (CRF) line and lab listings, and medical coding; highlights areas for medical review

3. Supports study-related committees by attending meetings, preparing meeting minutes, and maintaining all committee-related documents. May serve as a committee manager。

4. Uploads and manages documents collected for pre-enrollment review and endpoint adjudication into TrialEASTM.

5. Supports the Medical Affairs and Medical Operations departments and staff with the following duties:

• Performs file creation, retention, and maintenance (paper and electronic);

• Maintains Medical Monitor and Medical Operations study assignment roster, including tracking the assignment of back-up staff where appropriate;

• Maintains request for proposals (RFPs) spreadsheet including tracking awarded and lost projects pertaining to Medical Affairs;
• Initiats and follows up with study sites as necessary;
• Maintains the SharePoint web sites for Medical Affairs and Medical Operations by granting user access, creating new document libraries, and updating “out of office” calendar for department members.

6. Ensures compliance with the Code of Federal Regulations (CFR), HIPAA, state regulations, International Committee on Harmonization (ICH), and GCP guidelines, and sponsor Standard Operating Procedures (SOPs), and Work Instructions (WIs), where appropriate.

OTHER RESPONSIBILITIES:

Performs other work related duties as assigned. Minimal travel may be required (up to 25%).

Note: If there are additional responsibilities that are specific to an individual employee, department, country, or other grouping, please use the Job Description Addendum Template.

REQUIREMENTS:

BA/BS in the biological sciences or related discipline in the natural sciences/health care field, nursing degree, or equivalent combination of education and experience. Solid office/administrative experience. Nominal clinical research or medical clinic/hospital experience preferred. Good knowledge of ongoing protocol and disease related terminology and the drug development process, including database and medical terminology. Advanced proficiency in Microsoft Office Suite (Word, Excel, and PowerPoint), email, and voicemail. Strong customer service skills with effective written and verbal communication appropriate to a professional medical setting. Strong organizational, presentation, documentation, and interpersonal skills, as well as a team oriented approach. Excellent verbal, written, and communication skills. Ability to multitask to meet tight deadlines in a dynamic environment while providing attention to detail and high quality work.

Why Syneos HealthTM? Join a game-changing global company that is reinventing the way therapies are developed and commercialized. Created through the merger of two industry leading companies - INC Research and inVentiv Health - we bring together more than 21,000 clinical and commercial minds to create better, smarter, faster ways to get biopharmaceutical therapies to patients. Teaming with some of the most talented professionals in the industry, you'll gain exposure and work in a dynamic environment where you'll be supported with comprehensive resources including emerging technologies, data, science and knowledge sharing. Grow your career with a global company committed to shortening the distance from lab to life.