Clinical Trial Administrator
2 weeks ago
**Essential Job Duties**:
1) Document and track study activities using relevant forms and tools, as well as relevant Project Management Systems with guidance/support
2) Assist in the preparation of study and site specific materials in accordance with relevant SOPs
3) Complete minute taking and documentation for sponsor/external or internal teleconferences as requested
4) Assist in setting up and maintaining tracking systems/spreadsheet for e.g. study supplies
5) Maintain the Project Directory
6) Provide support for Investigator Meetings; track meeting attendees and/or other information regarding the Investigator Meeting
7) Provide support to project team (e.g. proof-reading and editing correspondence, mailings, shipping of study files, faxing and photocopying documents, assembling study documents, and arranging meetings, etc.)
8) Maintain Trial Master File documentation within the appropriate TMF platform, participate in TMF QC, as assigned, and track and /archive as applicable
9) Audit and CAPA tracking
10) Set up and maintain clinical investigator files and documentation
11) Liaise with vendors, as needed, for study conduct such as printing study materials and/or external systems access for study team members.
- Coordinate and plan study supply shipments with vendors
- Maintain and confirm shipment information such as courier tracking numbers and date of shipping and delivery
- Prepare/assemble/ship supplies to sites pre-SIV: Study File Notebooks, CRFs, other study-specific ancillary supplies (i.e. diary cards, patient visit reminders);
12) Generate reports as needed, for example CTMS site contact information list
13) Work with the In-House CRA and other project team members on reconciliation of data with CTMS.
14) General communications to sponsors, sites and internal team members via electronic mail or courier or telephone
15) Perform other administrative duties as assigned by Line Manager, Project Managers or Clinical Trial Lead.
**Minimum Required**:
- Minimum one (I) year administrative experience or equivalent training
- Good oral and written communication skills
- Good organizational and time management skills
- Computer literacy (Microsoft Office Suite (Word, Excel, PowerPoint)
**Labcorp is proud to be an Equal Opportunity Employer**:
As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
For more information about how we collect and store your personal data, please see our Privacy Statement.
-
Clinical Trial Administrator
2 weeks ago
Navi Mumbai, India Labcorp Full time**Essential Job Duties**: 1) Document and track study activities using relevant forms and tools, as well as relevant Project Management Systems with guidance/support 2) Assist in the preparation of study and site specific materials in accordance with relevant SOPs 3) Complete minute taking and documentation for sponsor/external or internal teleconferences...
-
Clinical Trial Administrator
2 weeks ago
Navi Mumbai, Maharashtra, India Labcorp Full timeEssential Job Duties:1) Document and track study activities using relevant forms and tools, as well as relevant Project Management Systems with guidance/support2) Assist in the preparation of study and site specific materials in accordance with relevant SOPs3) Complete minute taking and documentation for sponsor/external or internal teleconferences as...
-
Clinical Trials
2 weeks ago
Mumbai, Maharashtra, India Diabetes Unit KEM Hospital Pune Full timeClinical trials are the actual experimental studies in which human volunteers are included, after their consent, to test new treatments, instruments,Read More
-
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 Assistant
2 weeks ago
Mumbai, Maharashtra, India ICON Strategic Solutions Full timeICON plc is a leading healthcare intelligence and clinical research company. We take pride in creating a diverse and innovative work environment, and we invite you to be part of our journey to influence the future of clinical development.Clinical Trial AssistantLocation : Mumbai, On-siteResponsibilities:- Document collection and submission support- Vendor...
-
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 Trial Associate
1 week 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 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 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
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
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 Associate
1 week 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,...
-
Clinical Trial Coordinator I
3 weeks ago
Mumbai, India Thermo Fisher Scientific Full timeAt Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through...
-
Clinical Trial Assistant
2 months ago
Mumbai, Maharashtra, India Fortrea Full timeAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...