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Medical Content Developer/Clinical Study Specialist
3 weeks ago
As a skilled Medical Content Developer/Clinical Study Specialist, you will be responsible for developing high-quality clinical trial documents and regulatory compliant materials.
The ideal candidate will have experience in creating clear and concise key clinical trial documents, including protocols, Investigator's Brochures (IBs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), and Clinical Study Reports (CSRs).
You will also be responsible for translating complex scientific data into well-structured documents that support drug development and approval processes. Additionally, you will assist in crafting abstracts and manuscripts, demonstrating strong scientific communication skills.
Key responsibilities include preparation of protocols, CSRs, PIS-ICFs, and CRFs, understanding study objectives, designing the protocol, preparation and review of SOPs, and communicating with stakeholders to ensure effective documentation within timelines.
We are seeking an experienced professional who is committed to delivering high-quality documents that contribute to the success of clinical research and regulatory submissions.
- Required Skills and Qualifications:
- Proficient in developing key clinical trial documents
- Experience in translating complex scientific data into clear documents
- Strong scientific communication skills
- Ability to work effectively with stakeholders
Why You'll Love This Job:
This role offers the opportunity to work on high-profile projects, develop your skills as a medical content developer, and contribute to the success of clinical research and regulatory submissions.
What We Offer:
Competitive compensation package, opportunities for growth and professional development, and a collaborative work environment.
How To Apply:
Send your resume and cover letter to us, and we'll get back to you soon.
