Skip to main content

Advarra hiring fresher for research associate l position

Advarra hiring fresher for research associate l position .

Bengaluru - IND


Job details
Description
Primary Duties and Responsibilities

• Understand and interpret clinical trial study protocols to design and develop calendars. Understand and interpret clinical trial agreements and sponsor budgets to develop site budgets for the protocol.
• Design and develop case report forms for clinical trial study protocols
• Develop a familiarity with Advarra’s Clinical Trial Management Software (CTMS) and Electronic Data Capture (EDC) software to utilize related functionalities in the design and development of calendars, budgets, financials and case report forms.
• Work closely with reporting manager to complete daily/ weekly calendars, budgets, financials and/or case report forms design to meet with pre-determined quality criteria.
• Understand and utilize internal case management software and other reporting software to ensure that daily/weekly work assignments are appropriately tracked and completed.
• Actively participate in team meetings and contribute meaningfully to discussions related to specific customer cases and/or protocols.

Position Requirements:

• Knowledge of clinical research methodology, industry regulations and Good Clinical Practice guidelines related to human research.
• Expected to work independently, as well as in a team environment.
• Good organizational and administrative abilities
• Familiarity with MS Office and various business software
• Preferred: 0-1 year work experience in job areas such as: o Clinical trial coordinator at site
o Clinical data management
o Pharmacovigilance
o Records management






Comments

Popular posts from this blog

Job Title: Regulatory Affairs Specialist Company: Medifodil Pharmaceuticals

Job Title : Regulatory Affairs Specialist Company: Medifodil Pharmaceuticals Location: [Insert City/Remote] Employment Type: Full-time Role Overview Medifodil Pharmaceuticals is seeking a detail-oriented and experienced Regulatory Affairs Specialist to join our growing team. You will be responsible for managing complex regulatory submissions and navigating the requirements of international health authorities. We are looking for a professional who thrives in a cross-functional environment and is passionate about ensuring compliance in the global pharmaceutical market. Key Responsibilities Prepare and manage regulatory submissions for global markets. Liaise with international regulatory authorities to ensure timely approvals. Collaborate with cross-functional pharmaceutical teams to maintain product compliance. Stay updated on evolving international regulatory frameworks and guidelines. What We Offer Compensation: ₹6 LPA – ₹10 LPA (Commensurate with experience and industry ba...

Opportunity Alert: Walk-In Interviews at Glenmark Pharmaceuticals

Opportunity Alert: Walk-In Interviews at Glenmark Pharmaceuticals Goa Are you looking to take the next step in your pharmaceutical career?  Glenmark Pharmaceuticals Ltd. is hosting walk-in interviews for its Goa (Unit I) facility.  This is a fantastic opportunity for experienced professionals in Production and Packing to join a global leader in the industry.Below are the full details regarding the open positions, requirements, and interview schedule. Open Positions 1. Senior Officer – Production & Packing Sections: Compression, Granulation, Coating, Capsule filling, Wruster, Blister, and Bottle. Qualification: B. Pharm / M. Pharm / M.Sc (Regular/Full Time). Experience: 2 to 5 years. 2.      Jr officer production packing  Sections: Compression, Granulation, Coating, Capsule filling, Wruster, Blister, and Bottle. Qualification: I.T.I / Diploma (Regular/Full Time). Experience: 2 to 5 years.Note: Candidates must have experience in pharma units approved by r...

Medpace hiring fresher and experienced clinical Data Coordinator.

Medpace hiring fresher and experienced clinical Data Coordinator. Job Locations  India-TTC, Thane Belapur Road | India-TTC, Thane Belapur Road Category Data Management Job Summary Our clinical activities are growing rapidly, and we are currently seeking a full-time, office-based Data Coordinator to join our Data Management team in India, Mumbai. If you want an exciting career where you can develop and grow your career even further, then this is the opportunity for you. Responsibilities Track and maintain metrics regarding the status of the data within EDC systems Clean the clinical database, which includes generating and resolving data clarifications Reconcile clinical data Assist with support activities for the Data Management department Qualifications Bachelor’s degree in life science/ pharmacy/ health related field with strong attention to detail and working knowledge of Excel and Word; Knowledge of medical terminology and Clinical Research is preferred; and Good kn...