Clinical Research Coordinators job @ Clinexa Life Sciences

 

Clinexa Life Sciences Pvt Ltd is an ISO 9001:2008 Certified full-service Contract Research Organization (CRO) with extended clinical research capabilities having a distinguished investigator network throughout India offering comprehensive clinical research and site management services to Pharmaceutical and Biotechnology companies, Contract Research Organizations etc. Following the guidelines for re-engineering the clinical research enterprise as outlined in the NIH-Road Map for medical research we aim to contribute to accelerating and strengthening clinical research by adopting a systematic infrastructure that will better serve the evolving field of scientific discovery.

Job Title :

Clinical Research Coordinators

Job Description :

Primary responsibility is to ensure smooth, accurate progress of the project from the planning stage through study end (and often beyond) by acting as liaison to the investigator, the subject, the institution, and the sponsor.

Additional Skills Required :

• Knowledge of Indian and International Clinical trial regulations.
• Interest in research methodology.
• Detail oriented.
• Good organizational skills.
• Ability to work independently.
• Innovative and creative.
• Flexibility.
• People oriented.
• Good interaction skills with patients.
• Certification in clinical research preferred.

Eligibility :

B.sc / M.sc in Life science

Experience Required : 0-1 years

How to Apply :

Interested candidates can send their resumes to hr@clinexa.com

 

Biocon : opening for Freshers

Biocon is an integrated biotechnology enterprise focused on the development of biopharmaceuticals. With successful initiatives in drug discovery and development, bioprocessing, manufacturing and global marketing, Biocon delivers products and solutions to partners and customers in over 75 countries. Biocon has the defining science, world class capabilities and a focused vision to deliver the promise of innovative and affordable medicine to a waiting world. Today, Biocon together with group companies employs more than 5000 employees with approximately Rs 2500 crore turnover and is expected to grow further during the current financial year.

 

Job Title :

Junior Executive Insulin Manufacturing Life Science

Job Description :

• Support the manufacturing team and participate in shift operations as for example (Bioreactors, Chromatography systems, buffer preparation, clean equipment's, cleaning tanks, centrifuges, sterilization of equipment's, HPLC etc.)
• Adherence to Safety, Health and Environment measures.
• Calibration of weighing instruments in production.
• Monitoring and control of specific production operations.
• Adherence to available Standard Operating Procedures & product specifications.
• Entering data in Quality Records.
• Product handling and packaging.
• Adherence to cGMP.
• Reporting of product/system non-conformities, and implementation of corrective/ preventive actions in specific areas of operation.

Eligibility :

B.sc Biochemistry, Microbiology

Experience Required : 0-2 years

How to apply :

Interested candidates can send their resumes to human.resources@biocon.com or apply

 

Indian Pharmacists' Oath

Pharmacists' Oath

• I Swear by the code of Ethics of Pharmacy Council of India in relation to the community and shall act as an integral part of health care team.
• I shall uphold the laws and standards governing my profession.
• I shall strive to perfect and enlarge my knowledge to contribute to the advancement of pharmacy and public health.
• I shall follow the system, which I consider best for pharmaceutical care and counseling of patients.
• I shall endeavour to discover and manufacture drugs of quality to alleviate sufferings of humanity.
• I shall hold in confidence the knowledge gained about the patients in connection with professional practice and never divulge unless compelled to do so by the law.
• I shall associate with organizations having their objectives for betterment of the profession of Pharmacy and make contribution to carry out the work of those organisations.
• While I continue to keep this Oath inviolated, may it be granted to me to enjoy life and the practice of pharmacy respected by all, at all times!
• Should I trespass and violate this oath, may the reverse be my lot!

Current Openings @ Fortis

 

 

Quality Control (Bioanalytical Section)

Apply here

Role : Assist Head- Bioanalytical in ensuring GLP and applicable regulatory compliance to achieve and maintain desired quality standards Responsibilities : Ensuring strict compliance with GLP norms in the bioanalytical section Monitoring compliance with Standard Operating Procedures Checking documentation for every procedure carried out from Analysis to reporting of results Preparation of Standard Operation Procedures for various activities To coordinate monthly training sessions for the bioanalytical staff To impart training to all personnel for implementation of quality systems Preparation of the department for External Audits & Inspections Preparation of training schedule for the new employees Conduct of regular QA Audits to verify compliance to Quality Systems Clinical Study Coordination Apply here Role : Assists the clinical investigator in efficiently executing the logistics of all clinical studies at the CRO Responsibilities : Primary : To assist in preparation of protocol and its appendices To interact with the caterer to ensure timely provision of meals as per approved meal plans To ensure sufficient numbers of ICFs are available in the required languages to obtain the informed consent before start of the study To make logistical provisions required by the protocol: path lab, clinical supplies, water, meals, etc. To check vital signs sheet and adverse events monitoring sheets of subjects along with all raw data form To monitor safety parameters during clinical studies To write and revise SOPs and ensure compliance with all current policies and procedures To assist in compilation of raw data related to safety of subjects Secondary : To be available at centre during in house part of study to handle medical emergencies To check vital signs sheet and adverse events monitoring sheets of subjects To review medical screening records and ascertain suitability of subjects Volunteer selection, informed consent procedure as per defined procedure To conduct clinical examination of all subjects participating during all clinical studies Preparation of clinical report and study update Quality Control - Clinical Apply here Role : Assist the Head, Clinical Operations in implementing quality control activities by verifying the trial- related activities for fulfilling ICH-GCP, GLP requirements in all clinical studies at the CRO. Responsibilities : To assess and implement quality control measures at all levels to increase efficiency and work standard. To ensure studies are more compliant with SOP, Protocol and applicable regulatory guidelines. To conduct online checks during study to increase quality and to prevent sponsor and quality assurance observations. To impart training on relative SOPs’ and quality programme. To assist Head, Clinical Operations to maintain timelines in the conduct of study procedures and training. To conduct meeting and to discuss quality assurance audit observations and prevent recurrence. To review and modify the required clinical/general SOP as need arises. http://www.fortis-cro.com/jobs-at-fortis.html