Your browser does not support javascript! Please enable it, otherwise web will not work for you.

Clinical Research Associate @ RMSP Academy

Home > Bio Tech / R&D / ScientistPharmacist / Medical Representative

 Clinical Research Associate

Job Description

We are looking for an organized, flexible clinical research associate to oversee clinical trials. The clinical research associate will develop and outline trial protocols, establish trial sites, train site staff, and manage Investigational Product (IP) and trial materials. The clinical research associate will manage multiple aspects of the subjects' welfare. You will conduct regular site visits, generate and distribute internal and external newsletters, prepare final reports, and liaise with interested parties regarding all trial aspects. You will play a leading role in generating and overseeing documentation and records.

To be successful in this role, you should be able to recognize logistical problems and initiate appropriate solutions. Ideal candidates will be detail-oriented, have the ability to multitask, and be able to collaborate with various role players.
Clinical Research Associate Responsibilities:

    Creating and writing trial protocols, and presenting these to the steering committee.
    Identifying, evaluating, and establishing trial sites, and closing sites down on completion of the trial.
    Training site staff on therapeutic areas, protocol requirements, proper source documentation, and case report form completion.
    Liaise with the ethics committee regarding the rights, safety, and well-being of trial subjects.
    Ordering, tracking, and managing IP and trial materials.
    Overseeing and documenting IP dispensing inventory, and reconciliation.
    Protecting subjects confidentiality, updating their information, and verifying IP have been dispensed and administered according to protocol.
    Conducting regular site visits, coordinating project meetings, and writing visit reports.
    Implementing action plans for sites not meeting expectations.
    Liaising with regulatory authorities.
    Ensuring compliance with SOPs and local regulations, and ICH and GCP guidelines.
    Other tasks and responsibilities as needed.

Employement Category:

Employement Type: Full time
Industry: Medical / Healthcare
Role Category: Bio Tech / R&D / ScientistPharmacist / Medical Representative
Functional Area: Not Applicable
Role/Responsibilies: Clinical Research Associate

+ View Contactajax loader


Keyskills:   time management critical thinking stress management relationship management to attention detail

 Job seems aged, it may have been expired!
 Fraud Alert to job seekers!

₹ 50,000 - 1.0 Lakh/Yr

Similar positions

Clinical Data Coordinator

  • Techno Endura
  • 0 to 1 Yr
  • Multi-City, India
  • 1 month ago
₹ 4.0 - 5 Lakh/Yr

Clinical Data Associate

  • Techno Endura
  • 0 to 1 Yr
  • Multi-City, India
  • 2 mths ago
₹ Not Specified

Clinical Data Analyst

  • Techno Endura
  • 0 to 1 Yr
  • Multi-City, India
  • 2 mths ago
₹ Not Specified

Clinical Research Assistant

  • Techno Endura
  • 0 to 1 Yr
  • Multi-City, India
  • 2 mths ago
₹ Not Specified

RMSP Academy

Galaxy Consultancy is one of the established HRD consultants of South India with adequate and suitable infrastructureas well as skilled and professionally trained staffs. For the last more than one decade we have been handling many eminent organizations .And regularly taking care of their manpower r...