DAVA Oncology

DAVA Oncology is a fast-growing oncology-focused consulting company headquartered in Dallas, Texas. We are recruiting for a Medical Writer and Research Analyst to join our team remotely from India . This is a fully remote position , but working hours will be based on U.S. time zones , meaning evening and night shifts will be required. Our team members have the opportunity to work in a variety of areas, including but not limited to: clinical trial research and communications, drug or trial publication research and review, and oncology conference meeting reviews. Candidates with previous experience in the oncology therapeutic area are highly desirable. Responsibilities: Conduct secondary research and acquire information from internet sources, compiling it into content. Interpret, analyze, and compile proprietary data in a way that delivers a compelling scientific story. Research, write, edit, and proof protocols, reports, and publications . Maintain a strong scientific understanding of oncology (or the ability to quickly gain such understanding). Prepare materials for major cancer conferences and internal oncology meetings . Qualifications: At least 1 year of experience in oncology-focused research or writing is preferred; publication planning experience is a plus. Ph.D. in biology, biochemistry, organic chemistry, immunology, molecular biology, biotechnology, Pharm.D. , or other related fields. M.S. degree holders in the above fields with exceptional experience will also be considered. Authorship in prestigious, peer-reviewed journals is highly preferred. Experience in planning, writing, and reviewing study designs, protocols, data analysis, study reports, and regulatory documents is a plus. Industry experience (pharmaceutical companies, CROs, etc.) is highly preferred. Skills & Proficiencies: Strong written and oral communication skills ; ability to explain technical concepts clearly. Advanced knowledge of Microsoft Office Suite . Ability to work independently and collaboratively on multiple projects with tight deadlines. Highly motivated, organized, and detail-oriented self-starter. Availability to work U.S. hours (evening/night shifts in India). Show more Show less

Work Hours:U.S. time zones – requires evening/night shifts in India DAVA Oncology is a fast-growing oncology-focused consulting company headquartered in Dallas, Texas. We are recruiting for a Medical Writer and Research Analyst to join our team remotely from India . This is a fully remote position , but working hours will be based on U.S. time zones , meaning evening and night shifts will be required. Our team members have the opportunity to work in a variety of areas, including but not limited to: clinical trial research and communications, drug or trial publication research and review, and oncology conference meeting reviews. Candidates with previous experience in the oncology therapeutic area are highly desirable. Responsibilities: Conduct secondary research and acquire information from internet sources, compiling it into content. Interpret, analyze, and compile proprietary data in a way that delivers a compelling scientific story. Research, write, edit, and proof protocols, reports, and publications . Maintain a strong scientific understanding of oncology (or the ability to quickly gain such understanding). Prepare materials for major cancer conferences and internal oncology meetings . Qualifications: At least 1 year of experience in oncology-focused research or writing is preferred; publication planning experience is a plus. Ph.D. in biology, biochemistry, organic chemistry, immunology, molecular biology, biotechnology, Pharm.D. , or other related fields. M.S. degree holders in the above fields with exceptional experience will also be considered. Authorship in prestigious, peer-reviewed journals is highly preferred. Experience in planning, writing, and reviewing study designs, protocols, data analysis, study reports, and regulatory documents is a plus. Industry experience (pharmaceutical companies, CROs, etc.) is highly preferred. Skills & Proficiencies: Must be available to work during U.S. business hours (evening/night shifts in India). Strong written and oral communication skills ; ability to explain technical concepts clearly. Advanced knowledge of Microsoft Office Suite . Ability to work independently and collaboratively on multiple projects with tight deadlines. Highly motivated, organized, and detail-oriented self-starter. Availability to work U.S. hours (evening/night shifts in India). Show more Show less

Work Hours:U.S. time zones – requires evening/night shifts in India DAVA Oncology is a fast-growing oncology-focused consulting company headquartered in Dallas, Texas. We are recruiting for a Medical Writer and Research Analyst to join our team remotely from India . This is a fully remote position , but working hours will be based on U.S. time zones , meaning evening and night shifts will be required. Our team members have the opportunity to work in a variety of areas, including but not limited to: clinical trial research and communications, drug or trial publication research and review, and oncology conference meeting reviews. Candidates with previous experience in the oncology therapeutic area are highly desirable. Responsibilities: Conduct secondary research and acquire information from internet sources, compiling it into content. Interpret, analyze, and compile proprietary data in a way that delivers a compelling scientific story. Research, write, edit, and proof protocols, reports, and publications . Maintain a strong scientific understanding of oncology (or the ability to quickly gain such understanding). Prepare materials for major cancer conferences and internal oncology meetings . Qualifications: At least 1 year of experience in oncology-focused research or writing is preferred; publication planning experience is a plus. Ph.D. in biology, biochemistry, organic chemistry, immunology, molecular biology, biotechnology, Pharm.D. , or other related fields. M.S. degree holders in the above fields with exceptional experience will also be considered. Authorship in prestigious, peer-reviewed journals is highly preferred. Experience in planning, writing, and reviewing study designs, protocols, data analysis, study reports, and regulatory documents is a plus. Industry experience (pharmaceutical companies, CROs, etc.) is highly preferred. Skills & Proficiencies: Must be available to work during U.S. business hours (evening/night shifts in India). Strong written and oral communication skills ; ability to explain technical concepts clearly. Advanced knowledge of Microsoft Office Suite . Ability to work independently and collaboratively on multiple projects with tight deadlines. Highly motivated, organized, and detail-oriented self-starter. Availability to work U.S. hours (evening/night shifts in India).

Clinical Research Associate – Tuberculosis Initiative This role offers an opportunity to contribute to a healthcare initiative aimed at improving access to tuberculosis treatment, diagnostics, and patient care . The focus is on collaborating with leading hospitals and government TB treatment centers to enhance treatment delivery and optimize patient outcomes. The Clinical Research Associate (CRA) will play a key role in coordinating program activities, overseeing project implementations, and ensuring compliance with established protocols . The position involves working closely with medical professionals, healthcare institutions, and field teams to strengthen TB care initiatives. Primary Responsibilities Work with hospitals and treatment centers to support TB care initiatives, including patient management and treatment monitoring. Ensure adherence to clinical protocols and quality standards in TB treatment and diagnostic programs. Facilitate patient enrollment, data collection and patient follow ups at partner hospitals to track treatment outcomes and program impact. Coordinate with healthcare teams to optimize the use of medicines and diagnostics provided through the initiative. Conduct site visits to assess the implementation of TB treatment programs and identify areas for improvement. Gaps in medicines and other services at TB treatment centers and hospitals Engage with senior medical professionals and administrators to support the expansion and sustainability of TB programs. Monitor and document program activities , ensuring compliance with healthcare guidelines and best practices. Assist with reporting, analysis, and strategic planning to enhance the effectiveness of the initiative. Qualifications Master’s or PhD in life sciences, public health, clinical studies, or a related field . 2-3 years of experience in healthcare program management, infectious diseases, or tuberculosis treatment . Strong understanding of treatment guidelines, diagnostic protocols, and patient care standards . Ability to collect and analyze healthcare data , document findings, and communicate insights effectively. Excellent organizational and interpersonal skills to collaborate with hospitals, medical professionals, and public health stakeholders. Travel Requirement Up to 50% travel across India to partner hospitals and treatment centers for program coordination and assessment. Travel will involve train and air travel to key locations. Job Type & Location Full-time position , based in Delhi, India . Hybrid role with a combination of office-based coordination and field engagement .