Total 3 Health / Beauty / Fitness job vacancies in Ponneri,, Tamil Nadu

At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.

We are looking for an Associate Director, Medical Writing to join our A-team (hybrid*). As an Associate Director, Medical writing you will be responsible for writing, editing, and compiling written deliverables within the Allucent Consulting Business Unit. Deliverables are focused on the disciplines of chemistry, manufacturing, and controls (CMC); nonclinical; clinical; medical affairs; and/ or regulatory affairs. Deliverables may be for submission to regulatory agencies, sponsor us, or for publication or presentation. This position leads and contributes to scientific discussions regarding the planning, production, and review of written deliverables. The Associate Director, Medical Writing provides counsel to and may manage the medical writing team and ensures timely preparation of organized, well-written, and high quality deliverables.

The Associate Director, Medical Writing will serve on project teams in various capacities including but not limited to: Medical Writer, Assistant Consulting Project Lead, Consulting Project Lead, and Program Director. The Associate Director, Medical Writing may have one or more direct reports.  

In this role your key tasks will include:

• Writes, edits, and compiles written deliverables in the disciplines of chemistry, manufacturing, and controls (CMC); nonclinical; clinical; medical affairs; and/ or regulatory affairs for submission to regulatory agencies (e.g., U.S. Food and Drug Administration), sponsor use, or for publication or presentation.
• Leads or contributes to scientific discussions regarding the planning, production, and review of written deliverables.
• Performs literature searches and literature reviews, as assigned  Has knowledge, commensurate to experience, of industry best practices and Health Authority Regulatory Guidance & Regulationsofo preparation of regulatory filings through all phases of drug or device development and lifecycle management.
• Seeks professional development opportunities to maintain knowledge of regulatory requirements and industry best practices. May include relevant certifications (RAC, MWC, CMPP, CCRP) .
• Displays knowledge, commensurate to experience, of company templates, requirements, and resources related to the production of written deliverables. 
• Adheres to established company or sponsor practices or guidelines as directed by the project manag .
• Leads or assists in the development of templates and guidelines for regulatory and other written deliverables.
• Edits and guides the writing of clinical/scientific documents written by other team members or clients.  
• Mentors of less-experienced Medical Writers. 
• Commensurate with experience, represents the Medical Writing department in interactions with other departments and potential sponsors during business development activities   
• Commensurate with experience, provides guidance relate.d to written deliverables to project teams and sponsors, including advice on the structure and content of, and strategies for, written deliverables. 
• Associate Director with and without direct reports. 
• Actively supports staff learning & development. 
• Provides guidance and advises Project Leads and/or Project Team . 
• Adheres to project budgets and contracts including scope and scope changes, timelines, and active resource management. 
• Coaches, mentors, and develops reports on collaborative consulting. 
• Applies company policies and procedures to resolve issues   Identifies and mitigates risk .
• Assures good communication and relationships with current and prospective clients . 
• Assists in the evaluation of potential technologies .  
• Assists with the review of business development proposals and project cost structures and participates in bid defences.  
• Monitors and evaluates industry trends to leverage service offerings to ensure business growth (new opportunities and expansion of current client business).  
• Actively manages, develops, and strengthens client relationships; drives repeat business  
• Contributes to and participates in client evaluations.

To be successful you should possess:

• Candidates with a B.S., or equivalent degree, in a scientific area, with M.S., Ph.D., Pharm.D., M.D., or equivalent degree, in a scientific area strongly preferred 
• Regulatory knowledge of drug, biologic, or device development focusing on submission requirements for US, EU, and/ or Canada 
• Critical thinking and analytical skills, as well as strong written and verbal communication skills in English   
• Scientific and regulatory knowledge of drug, biological, or device development is desirable  
• Quality focus and attention to detail. 
• Emotional intelligence, customer-focused leadership, and good decision-making skills 
• Innovative, creative, and practical thinking, including the ability to problem-solve effectively 
• Proficient in relevant software including Microsoft Office (Word, PowerPoint, Excel), Adobe Acrobat (or other PDF software), and web-based meeting platforms 
• 6+ years of experience with regulatory requirements of US FDA, Health Canadaand/orr European authorities, including medical writing experience.

Benefits of working at Allucent include:

• Comprehensive benefits package per location
• Competitive salaries per location
• Departmental Study/Training Budget for furthering professional development
• Flexible Working hours (within reason)
• Opportunity for remote/hybrid* working depending on location
• Leadership and mentoring opportunities
• Participation in our enriching Buddy Program as a new or existing employee
• Internal growth opportunities and career progression
• Financially rewarding internal employee referral program
• Access to online soft-skills and technical training via GoodHabitz and internal platforms
• Eligibility for our Spot Bonus Award Program in recognition of going above and beyond on projects
• Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees

Disclaimers:

*Our hybrid work policy encourages a dynamic work environment, prescribing 2 days in office per week for employees within reasonable distance from one of our global offices.

“The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively “Allucent”). Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third-party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources.”

Key Responsibilities:

Leadership and Team Development:

Lead, Coach, and Mentor a Team: Provide guidance and support to a team of medical record reviewers, nurturing their professional growth and development.

Positive Work Environment:

Create a positive and inclusive work atmosphere by fostering recognition, empowerment, attentive listening, embracing diversity, and setting an exemplary standard for others.

Workload and Process Management:

Assign tasks to team members based on workload and prioritize tasks to meet defined timelines. Anticipate workload fluctuations and allocate resources effectively to achieve departmental objectives. Manage the review of complex medical records, ensuring precision and compliance with industry standards and regulations. Leading and overlooking the launch of new projects Reviewing client guidelines and making sure the project fulfills all the requirements.

Team Performance Monitoring:

Regularly assess team performance, provide constructive feedback, and conduct performance reviews. Identify training needs and coordinate training sessions to enhance team members’ skills and knowledge. Prepare regular reports on team performance, productivity, and quality metrics.

Quality Assurance:

Implement Quality Assurance Protocols: Develop and implement quality assurance protocols to uphold high standards of accuracy and completeness in record reviews.

Privacy and Security: Ensure team members adhere to privacy and security standards, including HIPAA compliance, when handling medical records.

Process Improvement:

Collaborate with project stakeholders to establish and refine processes, aiming for efficiency and effectiveness. Develop and maintain standard operating procedures (SOPs) to guide the team’s activities.

Communication and Collaboration:

Foster effective communication within the team and with other project stakeholders. Collaborate with project managers, clients, and other departments to ensure project goals are met.

Requirements:

• Graduates in Medical, Life sciences or related field.
  
• Minimum 1 year and Maximum 2 years of experience as a medical Record Reviewer.
  
• Exposure into the legal or medical malpractices related projects and not from the insurance based projects 
  
• Familiar With MS Word, Excel and PDF reader.

• Paid Sick leave, Casual leave and compensatory leave
  
• Statutory Benefits (PF)
  
• Paid Parental leaves based on the company norms (Maternity & Paternity)
  
• To help Employees’ Children Education support
  
• Profit Sharing Bonus
  
• Holidays based on Indian & UK
  
• Week offs on Saturdays and Sundays
  
• Health Insurance
  
• Internet Allowance
  
• Incentives/ Awards/ Gifts
  
• Employee Reward Program

Thirty Two Health Care is pleased to announce an exciting opportunity for a General Dentist to join our team. As a General Dentist, you will be responsible for providing comprehensive dental care to our patients, diagnosing and treating oral health issues, and educating patients on proper oral hygiene practices. Our dental practice is committed to delivering exceptional patient care and maintaining the highest standards of dental treatment. We provide our dentists with a modern and well-equipped dental office, a supportive team, and a collaborative work environment.

Responsibilities

• Performing routine dental examinations and screenings
• Diagnosing and treating oral diseases and conditions
• Creating treatment plans and providing recommendations for patient care
• Performing dental procedures such as fillings, extractions, root canals, and dental restorations
• Collaborating with dental specialists and other healthcare professionals to ensure comprehensive and coordinated patient care
• Educating patients on proper oral hygiene practices and post-treatment care
• Maintaining accurate and detailed patient records
• Keeping up-to-date with advancements in dental technology and treatment protocols

• Doctor of Dental Surgery (DDS) or Doctor of Dental Medicine (DMD) degree from an accredited dental school
• Completion of a general practice residency program (preferred)
• Valid state dental license
• Minimum of 2 years of experience as a General Dentist
• Proficiency in performing a wide range of dental procedures
• Excellent diagnostic and clinical skills
• Strong knowledge of current dental technology and treatment techniques
• Commitment to providing exceptional patient care
• Excellent communication and interpersonal skills
• Ability to work well in a team-oriented environment
• Attention to detail and strong organizational skills