Description Background and Purpose
Exciting Career Opportunity in Global Healthcare & Pharmaceutical Consulting
Are you passionate about driving healthcare innovation and supporting the pharmaceutical and medical device industry? Do you thrive in a fast-paced environment that involves global collaboration and potential travel to Europe? If so, we invite you to join our dynamic team at Precision HealthCare Consultants.
Precision partners with leading U.S. pharmaceutical and medical device companies, providing top-tier scientific, regulatory, and technical expertise to enhance healthcare solutions worldwide. Our team plays a pivotal role in supporting clinical research, compliance oversight, and global market expansion.
We are seeking skilled professionals to support remote surveillance activities and on-site engagements with our clients. This role offers an opportunity to contribute to critical healthcare initiatives, ensuring compliance, quality assurance, and operational excellence in the evolving pharmaceutical and medical device landscape.
Key Responsibilities:
- Provide technical and regulatory support to U.S. pharmaceutical and medical device companies.
- Conduct remote and in-person assessments to ensure adherence to industry regulations and best practices.
- Collaborate with cross-functional teams on clinical research and global healthcare initiatives.
- Offer strategic insights to improve market access and patient outcomes.
- Potential for international travel, particularly to Europe, to support business expansion and global compliance efforts.
Who Should Apply?
We are looking for professionals with expertise in healthcare consulting, clinical research, regulatory affairs, and pharmaceutical operations. If you have a passion for global healthcare impact and enjoy working in an innovative and collaborative environment, we encourage you to apply.
Join us in making a meaningful difference in the pharmaceutical and medical device industry—both in the U.S. and beyond!
🚀 Apply today and be part of our growing global team!
Open Position
- P/T (Per Diem) Global Senior Technical Advisor
This role will support the project as a Subject Matter Expert for HIV/TB Research, Monitoring and Evaluation.
Duties Include:
- Provide Technical Assistance and backstop in technical and operational research strategy for HIV/TB.
- Developing and Reviewing Monitoring Tool Resources
- Aid in capacity building
- Clinical analytics
- Project evaluation
Requirements:
- Bachelor’s Degree in Science; Prefer advanced degree in Public Health or related field
- Minimum 8+ years clinical research experience and monitoring in infectious disease, reproductive health, respiratory medicine, oncology, or chronic diseases
- Experience with multi-center clinical trials monitoring at local and U.S. domestical regional levels or with NIH. International monitoring a plus
- Excellent written communication skills
- Familiarity with:
- IRB policies and procedures
- CRF data verification
- Informed consent review
- IRB reporting
- Corrective and preventive action plan development
- GCP training
- Regulatory requirements as necessary
- CRA certification (ACRP, CCRA, SoCRA) highly preferred
- Strong experience in project planning, development of monitoring plan, and management
- Ability to serve as resource, detailed oriented with excellent management, communication, and organization skills
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