Maharashtra Clinical assistant Jobs – 113 Open Jobs Today

Safety Sciences Assistant Manager
Fortrea —Pune, Maharashtra
- Full-time
- Windows
- Microsoft Office
- Databases
10d
Assistant Manager - HR @ SRV Rajebahadur Hospital Nashik
SRV Rajebahadur Hospital LLP —Nashik, Maharashtra
- ₹45,000 - ₹50,000 a month
- Full-time
- Human resources
- In-person
Quick apply
11d
Assistant Manager - Pharmacy
Symbiosis International University —Pune, Maharashtra
- ₹35,000 - ₹45,000 a month
- Full-time
- Bachelor's degree
- In-person
- Diploma
- Health insurance
- Paid sick time
Quick apply
Billing Assistant - Govt. Scheme
Symbiosis International University —Pune, Maharashtra
- ₹16,000 - ₹25,000 a month
- Full-time
- Bachelor's degree
- Computer skills
- In-person
- Health insurance
- Paid sick time
Quick apply
2d
Physician Assistant
Jupiter Hospital —Pune, Maharashtra
- Night shift
- Medicine
- Bachelor's degree
- Communication skills
9d
BAMS DOCTOR FOR CLINICAL ASSISTANT JOB
DR. ANSHUMAN MANASWI —Mumbai, Maharashtra
- ₹30,000 - ₹40,000 a month
- Full-time
- English
- Bachelor's degree
- In-person
Quick apply
Resident Medical Assistant- (House Officer)
Bhaktivedanta Hospital & Research Institute —Mira Road, Thane, Maharashtra
- ₹30,000 - ₹35,000 a month
- Full-time
- Medicine
- In-person
- Health insurance
- Food provided
Quick apply
Centre Head Operations
Dr. Agarwal's Eye Hospital —Thane District, Maharashtra
- ₹50,000 - ₹1,00,000 a month
- Full-time
- Hospitality
- Marketing
- Master's degree
Quick apply
Clinical Assistant / Clinical Associate
Sir H. N. Reliance Foundation Hospital and Research Centre —Mumbai, Maharashtra
- Medicine
- Master's degree
Assistant Manager
EXL Service —Pune, Maharashtra
- Full-time
- Customer service
- Bachelor's degree
- Mentoring
10d
Operation Theatre Manager
Tieten Medicity Hospital —Thane District, Maharashtra
- ₹40,000 - ₹70,000 a month
- Full-time
- Nursing
- Microsoft Office
- In-person
- Paid time off
- Paid sick time
Quick apply
Physician Assistant-In charge
Jupiter Hospital —Pune, Maharashtra
- Night shift
- Medicine
- Bachelor's degree
- Communication skills
9d
Clinical Assistant – (ICU/ PICU/ NICU/ER/ CRR/ Ward)
Sahyadri Hospitals —Pune, Maharashtra
Clinical Assistant
Dr. Roy Health Solutions Clinic —Mumbai, Maharashtra
- ₹10,000 - ₹13,000 a month
- Full-time
- Vital signs
- English
- Plumbing
Quick apply
Team Member - Case Management
Aditya Birla Group —Maharashtra
- Microsoft Powerpoint
- Medicine
- Microsoft Excel
Assistant Product Manager
B. BRAUN MEDICAL (INDIA) —Mumbai, Maharashtra
- B.Sc
- Master's degree
- Bachelor's degree
- Work from home
- Flexible schedule
Assistant Audiometrist and speech therapy technician
Healing Life Rehab clinic —Thane District, Maharashtra
- ₹15,000 - ₹20,000 a month
- Full-time
- Anatomy knowledge
- In-person
- Diploma
- Flexible schedule
- Food provided
Quick apply
5d
Clinical Assistant
Meadowlark Speciality & Super Speciality Pvt Ltd —Fatimanagar, Pune, Maharashtra
- ₹30,000 - ₹50,000 a month
- Full-time
- ICU experience
- Patient care
- In-person
Quick apply
1d
Registered General Nurse
BHARATI PRAKASH BHAYANI —Lower Parel, Mumbai, Maharashtra
- ₹45,000 - ₹70,000 a month
- Full-time
- English
- In-person
- Communication skills
Quick apply
Clinical Assistant
Jupiter Hospital —Kalyan-Dombivli, Maharashtra
- ₹50,000 - ₹80,000 a month
- Full-time
- Medicine
- Bachelor's degree
- In-person
- Health insurance
- Flexible schedule
Quick apply

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Safety Sciences Assistant Manager

Fortrea -
Pune, Maharashtra

Apply Now

Job details

Full-time
10 days ago

Qualifications

Windows
Microsoft Office
Databases
Quality assurance
Data entry
Research & development
Communication skills

Full job description

Job Overview:

Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process which may include safety data collected from clinical trials and/or post marketing setting (i.e., unsolicited reports). Manage and process expeditable adverse events to the required standard and submit them to the client and the regulatory agencies (if required) within the agreed/stated timelines. Responsible for providing this service to clients either as a support function to the client project groups or as stand-alone business. Responsible to provide all clients, both internal and external, with the appropriate quality of service in a safe and cost-effective manner. He/she will be expected to comply with the legal requirements of the Health and Safety at Work Act 1974, the COSHH regulations 1989 and the EC (European Commission) Directives 1992/3 as documented in the Company’s Health and Safety Manual.

Summary of Responsibilities:

Manage the receipt and processing of all adverse event reports reported either spontaneously from any source or solicited from a clinical trial including safety database entry, AE review, write patient narratives with coding, follow-up of missing information, listed assessment against appropriate label (for Marketed products, if applicable).
Manage submission of expedited SAE reports to clients, Regulatory Authorities, Ethics Committees, investigators, 3rd party vendors, Partner and Labcorp project personnel, if required and as agreed with client during study set-up, within study specified timelines.
Ensure all cases that require expediting reporting to worldwide Regulatory Agencies or other recipients are prioritised for processing and submission within the regulatory and/or study specific applicable timelines.
Prepares timely pharmacovigilance reports for products and safety issues, including Individual Case Summary Reports (ICSRs) of Serious Adverse Events (SAEs), Annual IND reports, European Annual Safety Reports (ASRs), Development Safety Update Report.
(DSUR), Periodic Reports (PRs) line listings, and aggregate reports.
May execute routine quality review of AE reports and aggregate reports for other members of the group ensuring that case processing and data quality meet global regulatory compliance needs including audit support.
Maintain a strong understanding of Labcorp’s safety database conventions or client-specific database conventions, as appropriate.
Participate in signal detection, trend and pattern recognition activities, as appropriate.
Prepares timely pharmacovigilance reports for products and safety issues, including Individual.
Case Summary Reports (ICSRs) of Serious Adverse Events (SAEs), Annual IND reports, European Annual Safety Reports (ASRs), Development Safety Update Report (DSUR), Periodic Reports (PRs) line listings, and aggregate reports.
Begin to participate and demonstrate leadership on projects which enhance team and/or division performance. This includes acting as a lead contact for projects including global projects ensuring communication and process harmonization.
Work with Data Management or client on reconciliation of safety databases, if appropriate.
Monitor workflow for assigned studies/programs to ensure all deadlines are met.
Prepare and deliver safety presentations- o Serious Adverse Event reporting at Investigator meetings o Client capabilities meetings, as appropriate o “Department Overview” to internal clients.
Maintains a comprehensive understanding of Labcorp PSS Standard Operating Procedures (SOPs), Work Instructions (WI), guidance documents and directives associated with safety management, reporting and pharmacovigilance.
Participate or contribute to the development of departmental Work Instructions (WI) and Standard Operating Procedures (SOPs), as appropriate.
Participate in the generation of monthly status and other project-specific reports ensuring the quality and accuracy of metrics/data provided.
Support/train less experienced safety staff in all aspects of case-handling, adverse event reporting and other work, as needed and contribute towards training material development and updates.
Contribute to preparation of Safety Management Plans (SMPs), Reconciliation Plans and other safety- specific plans under supervision.
Responsible for making decisions regarding adverse event reporting within the guidelines of each specific project.
Assist PSS management to identify out of scope work.
Actively participates in project team and client meetings and liaise with clients, where appropriate.
Participate in client or regulatory audits, and support preparation if needed.
Actively support quality issue resolution and implementation of process improvement initiatives/activities.
Assist in the review of cumulative safety data for submission to Drug Safety Monitoring Boards (DSMBs), regulatory authorities or clients.
Assist with the set-up of, and the provision of data to Safety Committees/DSMBs and assist in the co-ordination of endpoint committees, as required.
Build and maintain good PSS relationships across functional units.
Demonstrate role-specific Competencies and company values on a consistent basis.
Available for travel 10% of the time including overnight stays as necessary consistent with project needs and office location.
All other duties as needed or assigned.

Qualifications (Minimum Required):

- Safety experience includes actual experience processing AE/SAE reports, generating narratives, queries, working within safety databases, and experience with regulatory submissions.
** Relevant experience includes experience in the pharmaceutical, biotechnology, or CRO industry, working in related areas such as Medical Affairs, Clinical Data Entry and Clinical Data Management, Clinical Data Monitoring, Regulatory Affairs, or Quality Assurance.
Fortrea may consider relevant and equivalent experience in lieu of educational requirements.

Experience (Minimum Required):

Good verbal, written and presentation skills.
Good communication.
Ability to interact and influence with line and middle management, staff and external contacts on a functional and tactical level.
High degree of accuracy with attention to detail.
Functions as a team player.
Ability to present and share useful business information across departments and functions.
Ability to anticipate and identify problems and take appropriate action to correct.
Knowledge of medical and drug terminology.
Knowledge of Good Clinical Practice (GCP) related to clinical safety documentation.
Knowledge of ICH Guidelines.
Knowledge of Medical Device reporting desirable.
Knowledge of worldwide regulatory requirements and reporting of adverse event for both marketed and investigational products.
Good knowledge and understanding of industry and R and D processes and objectives.
Ability to work independently with minimal supervision.
Good keyboard skills, preferably with knowledge of MS office and Windows would be beneficial.

Preferred Qualifications Include:

Office environment.

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Refine Your Search

clinical assistant jobs in maharashtra

Safety Sciences Assistant Manager

Assistant Manager - HR @ SRV Rajebahadur Hospital Nashik

Assistant Manager - Pharmacy

Billing Assistant - Govt. Scheme

Physician Assistant

BAMS DOCTOR FOR CLINICAL ASSISTANT JOB

Resident Medical Assistant- (House Officer)

Centre Head Operations

Clinical Assistant / Clinical Associate

Assistant Manager

Operation Theatre Manager

Physician Assistant-In charge

Clinical Assistant – (ICU/ PICU/ NICU/ER/ CRR/ Ward)

Clinical Assistant

Team Member - Case Management

Assistant Product Manager

Assistant Audiometrist and speech therapy technician

Clinical Assistant

Registered General Nurse

Clinical Assistant

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