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Open nowFirst seen 6 days ago

Research Assistant, Medical Affairs San Diego, CA (Hybrid)

ESRhealthcare and EXEC STAFF RECRUITERS1,405 open roles

Where
San Diego, California, United States
Work mode
Hybrid
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Your applicationOpen nowResearch Assistant, Medical Affairs San Diego, CA (Hybrid)ESRhealthcare and EXEC STAFF RECRUITERS · San Diego, California, United States

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  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

  4. CV RocketApplied on ESRhealthcare and EXEC STAFF RECRUITERS's own form.

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The clock on this job

Early applications get read.

12.3% of postings close within 7 days. Measured by our own scanner across the market.

Share of postings closed within
  1. 2.1%1 day
  2. 4.5%3 days
  3. 12.3%7 days
  4. 19.7%14 days
  5. 35.6%30 days
  6. 58.0%60 days
This job: first seen 6 days ago

The posting

Research Assistant, Medical Affairs San Diego, CA (Hybrid)

Job Duration: 06 Months

Position Overview:

We are seeking a motivated and detail-oriented Research Assistant to join our Medical Affairs team. The Research Assistant will play an important role in supporting our account-level data initiative to help healthcare providers evaluate glycemic outcomes, gain insights into patterns of settings and outcomes, and identify optimization opportunities. This role will also support various research projects and initiatives aimed at enhancing patient care and advancing medical knowledge. The ideal candidate will be passionate about medical research, eager to learn, and ready to contribute to a dynamic team.

Responsibilities:

The primary responsibility will be to create customized Powerpoint presentations of data from a requested account using a Dashboard and standardized template, which will be used by field medical to faciliate discussions with healthcare providers.

Assist in the preparation of research reports, presentations, posters, abstracts, and publications.

Conduct proofreading, formatting, and data validation for research and publications deliverables.

Submit scientific manuscripts and conference abstracts through the relevant online portal, ensuring accuracy and completeness of submissions.

Coordinate meetings between internal and/or external investigators and team members on research and publications projects to ensure seamless collaboration

Manage review and approval of publication deliverables through the appropriate platform (Veeva MedComms, Arena, DocuSign, email, etc.)

Assist the real-world evidence research team in maintaining documentation for internal research projects

Participate in research projects as assigned, and maintain accurate records of research findings and manage research documentation

Conduct literature reviews and prepare reports on findings to support manuscripts and clinical study design

Maintain the team bibliography, shared reference library (EndNote or similar), and shared directory of past presentations and publications

Provide support for team conference activities, such as booking meeting rooms, coordinating meetings with key opinion leaders, coordinating ad boards, and supporting conference notetaking and report development

Ensure compliance with regulatory and ethical standards in all research activities.

Key Decision Rights:

Authority to recommend changes to research protocols and methodologies.

Responsibility for ensuring data accuracy and integrity in research documentation.

Ability to prioritize tasks and manage time effectively to meet project deadlines.

Participation in team meetings to provide insights and recommendations on research progress and findings.

Collaboration with cross-functional teams to align research activities with organizational goals.

Required Leadership/Interpersonal Skills & Behaviors:

Proactive and self-motivated with a positive attitude

Ability to communicate complex information clearly and concisely

Flexibility and adaptability in a fast-paced environment

Ability to influence and motivate others to achieve project goals

Strong ethical standards and integrity

Ability to work independently and as part of a team

Commitment to continuous learning and professional development

Required Skills and Competencies:

Strong writing and proofreading skills

Attention to detail and accuracy in data presentation

Excellent organizational and time management abilities

Basic understanding of clinical research methodologies and protocols

Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)

Ability to manage multiple tasks and projects simultaneously

Adaptability and willingness to learn new techniques and procedures

Education and Experience:

Bachelor's degree or its foreign equivalent is required.

A post-secondary degree (e.g. Master's) in a science field or public health is highly preferred

1-2 years of related experience in a research position at a medical device or biotechnology company, clinical research organization, or research institution (or the equivalent education and experience)

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