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Your Recruitment Specialist
Click on this paragraph.
Designation – Clinical Research Coordinator
Location – Thane Mumbai (Western line)
1. Education : B Pharm/M Pharm
2. Salary : Hike on current salary
3. Experience: 1-2 Years
§ Fresher :18-25K (Depends on Interview and Knowledge)
§ Experience: 20-25% hike on current salary
IF
Clinical Research Coordinator
§ Fresher :13-20K (Depends on Interview and Knowledge)
§ Experience: 20-25% hike on current salary
Job Responsibilities: Participates in the investigator recruitment process. Performs initial
qualification visits of potential investigators. Evaluates the capability
of the site to successfully manage and conduct the clinical study,
both clinically and technically.
Works with the Study Start-up Group to coordinate activities with
the site in preparation for the initiation of studies. Obtains regulatory
documentation for successful implementation, monitoring, and
evaluation of clinical trials. Works with Study Start-up Group and
site staff to obtain regulatory (EC) approval of study specific
documents.
Performs study initiation activities, reviewing with the site personnel
the protocol, regulatory issues, study procedures, and provides
training on completion of the eCRF; monitoring activities and study
close-out activities.
Trains site staff on the EDC system and verifies site computer
system.
Conducts periodic site file audits to ensure compliance with GCPs
and company’s standard operating procedures.
Assures adherence to Good Clinical Practices, investigator integrity,
and compliance with all study procedures through on-site monitoring
visits. Performs validation of source documentation as required by
sponsor. Prepares monitoring reports and letters in a timely manner
using approved company /sponsor forms and reports.
Documents accountability, stability and storage conditions of
clinical trial materials as required by sponsor. Performs
investigational product inventory. Ensures return of unused
materials to designated location or verifies destruction as required.
2
Reviews the quality and integrity of the clinical data through (1) in
house review of electronic CRF data and (2) on-site source
verification. Works with sites to resolve data queries.
Reviews protocols, eCRFs, study manuals and other related
documents, as requested by Clinical Trial Manager.
Serves as primary contact between the company and investigator;
coordinates all correspondence; ensures timely transmission of
clinical data with the study site and technical reporting, as requested.
Assists with final data review and query resolution through database
lock.
Performs study close-out visits.
Assists with, and attends, Investigator Meetings for assigned studies.
May serve as mentor for new clinical study monitors.
Authorized to request site audits for reasons of validity.
#customerresearchassociate #researchassociate #mumbaijob #mumbaijobs
Interested candidates kindly forward your updated CV on hr5@tasolutions.in given mail ID with your current and expected CTC or call on 9569909808 if not interested we will really appreciate it if u forward this position to your friends.
Sr. Medical Writer
Location – Thane Mumbai (Western Line)
1. Education : M Pharm (Pharmacology) /BHMS/BAMS
2. Salary : Hike on current salary
3. Experience: 1-3 Years
Salary range:
Sr. Medical Writer
§ Experience (more than 1-2 years :18-25K (Depends on Interview and Knowledge)
§ Experience (more than 3-4 years) – 20-25% hike on current salary
Job Responsibilities:
1. Drafting & Preparation of Phase I, II, III & IV protocol,
synopsis, PIS for various therapeutic areas such as
respiratory, diabetes mellitus, pain, antimicrobials,
cardiovascular and other specialties for India and global
submissions.
2. Writing CSR, IBs, SmPCs, PIs, PILs.
3. Project assignment and timeline to CRA’s -Operation team,
discussion with KOL and finalization of scientific study
Documents as per requirements
4. Literature search, systemic review of data and its analysis so
as to be up to date with latest breakthrough in the therapeutic
area.
5. Working closely with physicians and senior scientists for
study designs and protocol development to influence the
clinical pharmacology strategy in support of drug
development.
6. Preparing presentations, posters, research articles, abstract,
and manuscripts for publication purpose.
7. Activities as and when required.
#mumbaijobs #medicalwriter #medicalwriting
Interested candidates kindly forward your updated CV on hr5@tasolutions.in given mail ID with your current and expected CTC or call on 9569909808 if not interested we will really appreciate it if u forward this position to your friends.
Designation – Tender Lead And Tech Support
Experience – 2-3 years drafting experience
Salary -Upto 5 LPA
Location – Parwanoo
Work Timings 9 Am to 6 PM
Days – 6 days working
Qualification – Graduate
RESPONSIBILITIES
1. GeM- Tender Filling, Brand Approval, Vendor Management, OEM Management, Vendor Assessment,
Product Publishing.
2. Tender Work – Searching & filing state tenders, filling global tender and inquiring in other countries.
3. Responsible for drafting and sending out representation letters for queries and clarification to the
procuring/indenting entity
4. Responsible for end-to-end documentation related to pre and post TENDER requirements.
5. Market Intelligence – Calling customers and collecting market intelligence & Post Market
Surveillance (PMS) data under the guidance of Consumer & Regulatory Affairs teams.
6. Consumer Delight – Handling automated customer support via tech tools and getting complaint
tickets closed by plant under the guidance of Regulatory Affairs.
7. Secondary Research – Good with google search. Experience with running automated/mass
communications across various platforms, such as, email, LinkedIn, WhatsApp, etc.
#tender #tenders #tenderexecutive #Gem #govtemarkeplace #jobsinchndigarh #parwanoojobs #chandigarhjobs #chdjob #jobs #job
If interested can forward your updated resume on hr5@tasolutions.in and can directly contact us on 9023404909 also can provide our reference to your friends and colleagues
