![OneStudyTeam](https://media.trabajo.org/img/noimg.jpg)
Trial Design Associate
2 weeks ago
At OneStudyTeam (a Reify Health company), we specialize in speeding up clinical trials and increasing the chance of new therapies being approved with the ultimate goal of improving patient outcomes. Our cloud-based platform, StudyTeam, brings research site workflows online and enables sites, sponsors, and other key stakeholders to work together more effectively. StudyTeam is trusted by the largest global biopharmaceutical companies, used in over 6,000 research sites, and is available in over 100 countries. Join us in our mission to advance clinical research and improve patient care.
**One mission. One team. That's OneStudyTeam.**
**Job Type**: Contract 9-months
By joining as a **Trial Design Associate**, you will have the important responsibility of ensuring that clinical research professionals have an overwhelmingly positive, valuable experience when using OneStudyTeam's SaaS products. In streamlining our trial configuration processes, ensuring thorough QA of your own and the team's work, and seamlessly supporting our Sponsor Success team to ensure top-notch implementation of our products, you will have an impact on the progression of clinical trials.
**What You Will Be Working On**:
- Learn and develop deep expertise in Reify Health's cloud-based SaaS product(s).
- Set up the platform environment in preparation for trial implementation and new product implementation and provide feedback and suggestions (both internally and, when necessary, externally) on optimal design based upon the protocol
- Maintain system configuration according to customer feedback and protocol amendments.
- Provide QA assistance across the Trial Design team to ensure consistent, high quality product implementation
- Support a streamlined customer onboarding experience and provide additional oversight and quality assurance of StudyTeam across a multitude of departments.
**What You Bring to OneStudyTeam***:
- 1+ year of relevant experience in a clinical research setting.
- BA or BS, degree in business, science or related field, or AA degree and/or commensurate experience in relevant field(s).
- Experience working directly with clients (internal and/or external) and championing their long-term success.
- Proven experience researching, learning, and utilizing new technologies and software.
- Prior experience with a CTMS or other clinical research software tool preferred.
- Excellent communication (written and verbal), collaboration, and presentation skills.
- Ability to problem solve, think analytically, and be metric-driven.
- Ability to thrive in a fast-paced, start-up environment - you are comfortable with ambiguity and find no job too big or small.
- Extensive experience working with Excel and PowerPoint.
- Excellent organizational skills and impeccable attention to detail.
- Solution-oriented thinking, a zest for learning, and a willingness to help whenever needed.
- Business-level fluency in English
- We value diversity and believe the unique contributions each of us brings drives our success. We do not discriminate on the basis of race, sex, religion, color, national origin, gender identity, age, marital status, veteran status, or disability status._
**_ Note_**_: OneStudyTeam_ is unable to sponsor work visas at this time. If you are a non-U.S. resident applicant, please note that OST works with a Professional Employer Organization._
- As a condition of employment, you will abide by all organizational security and privacy policies._
-
Clinical Trial Associate
2 weeks ago
Mumbai, Maharashtra, India Ortolan Full timeClinical Trial Associate Mumbai or Vadadora, India (hybrid: 3 days office, 2 days home) Salary: Competitive + Benefits + Bonus If you are an agile, committed, and innovative clinical trial professional then we want to hear from you Join us to help improve peoples' lives and make healthcare better for everyone Why Pharmanovia? Pharmanovia is...
-
Clinical Trial Associate
2 weeks ago
Mumbai, Maharashtra, India Atnahs Full timeMumbai or Vadodara, India (hybrid: 3 days office, 2 days home):Salary:Competitive + Benefits + Bonus:If you are an agile, committed, and innovative clinical trial professional, then we want to hear from youJoin us to help improve peoples' lives and make healthcare better for everyoneWhy Pharmanovia?:Pharmanovia is a dynamic, fast-growing international...
-
Clinical Trial Associate
2 weeks ago
Mumbai, Maharashtra, India Atnahs Full time**Vadodara or Mumbai, India (hybrid: 3 days office, 2 days home)**: **Salary: Competitive + Benefits + Bonus**: If you are an agile, committed, and innovative clinical trial professional, then we want to hear from you! Join us to help improve peoples’ lives and make healthcare better for everyone! **Why Pharmanovia?**: Pharmanovia is a dynamic,...
-
Trial Master File Associate
1 week ago
Mumbai, India BIORASI LLC Full time**We are Growing**! Let us support your career journey the Biorasi way. Innovative, Collaborative, Dynamic and Evolving. Capitalizing on your strengths while encouraging work-life balance. Biorasi is an award-winning, customer-focused, full-service clinical research organization, and we are unlike any CRO you’ve ever heard of. Biorasi is looking for top...
-
Trial Master File Associate
2 weeks ago
Mumbai, Maharashtra, India BIORASI LLC Full timeWe are Growing Let us support your career journey the Biorasi way. Innovative, Collaborative, Dynamic and Evolving. Capitalizing on your strengths while encouraging work-life balance. Biorasi is an award-winning, customer-focused, full-service clinical research organization, and we are unlike any CRO you've ever heard of.Biorasi is looking for top performers...
-
Clinical Trial Associate
2 weeks ago
Mumbai, India Novartis Full time100,000+ That’s how many patients participate in our clinical trials at any given time. GCO is Novartis’ powerhouse of Global Clinical Operations, redesigned to enable faster trial recruitment and enhanced trial delivery resulting in more timely access for patients to potential novel treatments. Every day, we are the link between science and medicine -...
-
Clinical Trial Associate
4 days ago
Mumbai, Maharashtra, India Atnahs Full time**Mumbai or Vadodara, India (hybrid: 3 days office, 2 days home)**: **Salary: Competitive + Benefits + Bonus**: If you are an agile, committed, and innovative clinical trial professional, then we want to hear from you! Join us to help improve peoples’ lives and make healthcare better for everyone! **Why Pharmanovia?**: Pharmanovia is a dynamic,...
-
SAS/PH- Clinical trial analysis
2 weeks ago
Mumbai, Maharashtra, India Anicalls (Pty) Ltd Full timeExcellent understanding of the statistical principles underlying clinical trials Excellent statistical skills. candidates that are Statistical SAS, R programmers, and separately, we need pharmaceutical clinical trial statisticians. Excellent understanding of the regulatory issues associated with the reporting of clinical data in the submission process
-
Clinical Trial Medical Writer
2 weeks ago
Mumbai, Maharashtra, India Hansa MedCell Full timeWe are looking for a skilled Clinical Trial Medical Writer!Experience: 3+ years working in the field of clinical trial medical writingDevelop case report formats, protocol letters, and record forms crucial for clinical trialsPrepare all required documentation for the initiation, execution, and completion of clinical trialsConduct literature reviews and...
-
Clinical Trial Medical Writer
3 weeks ago
mumbai, India Hansa MedCell Full timeExperience: 3+ years in clinical trial medical writingResponsibilities:Develop case report formats, protocol letters, and record forms essential for clinical trials.Prepare all necessary documentation for clinical trial initiation, execution, and completion.Conduct literature reviews and data analysis to support trial design and manuscript development.Draft...
-
Clinical Trial Medical Writer
1 month ago
Mumbai, India Hansa MedCell Full timeExperience: 3+ years in clinical trial medical writing Responsibilities: Develop case report formats, protocol letters, and record forms essential for clinical trials.Prepare all necessary documentation for clinical trial initiation, execution, and completion.Conduct literature reviews and data analysis to support trial design and manuscript...
-
Clinical Trial Medical Writer
1 month ago
mumbai, India Hansa MedCell Full timeExperience: 3+ years in clinical trial medical writing Responsibilities: Develop case report formats, protocol letters, and record forms essential for clinical trials. Prepare all necessary documentation for clinical trial initiation, execution, and completion. Conduct literature reviews and data analysis to support trial design and manuscript...
-
Clinical Trial Medical Writer
1 month ago
Mumbai, India Hansa MedCell Full timeExperience: 3+ years in clinical trial medical writing Responsibilities: Develop case report formats, protocol letters, and record forms essential for clinical trials.Prepare all necessary documentation for clinical trial initiation, execution, and completion.Conduct literature reviews and data analysis to support trial design and manuscript...
-
Clinical Trial Medical Writer
4 weeks ago
Mumbai, India Hansa MedCell Full timeExperience: 3+ years in clinical trial medical writing Responsibilities: Develop case report formats, protocol letters, and record forms essential for clinical trials. Prepare all necessary documentation for clinical trial initiation, execution, and completion. Conduct literature reviews and data analysis to support trial design and manuscript...
-
Clinical Trial Medical Writer
4 weeks ago
Mumbai, India Hansa MedCell Full timeExperience: 3+ years in clinical trial medical writing Responsibilities: Develop case report formats, protocol letters, and record forms essential for clinical trials.Prepare all necessary documentation for clinical trial initiation, execution, and completion.Conduct literature reviews and data analysis to support trial design and manuscript...
-
Clinical Trial Medical Writer
3 weeks ago
Mumbai, India Hansa MedCell Full timeExperience: 3+ years in clinical trial medical writing Responsibilities: Develop case report formats, protocol letters, and record forms essential for clinical trials.Prepare all necessary documentation for clinical trial initiation, execution, and completion.Conduct literature reviews and data analysis to support trial design and manuscript...
-
Clinical Trial Medical Writer
1 month ago
Mumbai, India Hansa MedCell Full timeExperience: 3+ years in clinical trial medical writingResponsibilities:Develop case report formats, protocol letters, and record forms essential for clinical trials.Prepare all necessary documentation for clinical trial initiation, execution, and completion.Conduct literature reviews and data analysis to support trial design and manuscript development.Draft...
-
Clinical Trial Monitor
2 weeks ago
Mumbai, Maharashtra, India Bristol-Myers Squibb Full time**Working with Us** Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...
-
Clinical Research Associate
2 weeks ago
Mumbai, India Statistical Pharma Full timeSpecific duties can vary depending on the company, but clinical research associates will generally be required to: - Develop trial procedures, methodology and instructions for clinical trials staff, as well as design data collection tools (case report forms) - Manage study supplies, drug supplies and drug accountability (and prepare study drugs for...
-
Clinical Research Associate
1 month ago
Mumbai, India REGROW BIOSCIENCES Full timeOverview: As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements, and industry standards throughout the trial process. Responsibilities: 1 . Trial...