medical affairs specialist

Bayer

<p></p><div><p><b>At Bayer we&rsquo;re visionaries, driven to solve the world&rsquo;s toughest challenges and striving for a world where ,Health for all, Hunger for none&rsquo; is no longer a dream, but a real possibility. We&rsquo;re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining &lsquo;impossible&rsquo;. There are so many reasons to join us. If you&rsquo;re hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there&rsquo;s only one choice.</b></p><br>
<p></p>
<p><b>
Medical Advisor</b></p><p></p><p><b><br>
POSITION PURPOSE:</b></p>
<p>
The position is responsible for the medical and scientific support, including technical advice to the Business Units and Pharmacovigilance/ Medical Information and Clinical Research teams in their assigned therapeutic areas. This is crucial in view of the complex marketing environment in India due to the presence of generic players and self-pay nature of the market. The position holder oversees the Medical Affairs function in India in their assigned therapeutic/product areas and cooperates with (if applicable) Regional Medical Affairs functions and relevant Global Medical Affairs functions.</p>
<p>
This position holder is responsible for ensuring that marketing and sales functions have appropriate medical scientific support and training (the latter in co-operation with the Training department). Toenable this support, product and development project information is to be kept up to date based on internal publications and communication with regional and global Medical Affairs functions as well as based on review of pertinent scientific publications. In addition to this, the position holder is responsible for the review process of promotional materials in the respective area according to the global SOP and local laws and compliance. The tasks also include monitoring of medical marketing activities of competitors locally and worldwide and close interaction especially with regional medical affairs functions.</p>
<p>
The position holder will further support regulatory, PV/MI and CR teams in medical scientific questions and prepare and give internal (mainly marketing and sales functions) and possibly external presentations (local advisory board meetings, launch symposia and others) to enhance the medical knowledge of development projects and marketed products. This also includes interaction and relationship-building with Thought Leaders (TLs &ndash; Key HCPs).</p>
<p><b>
YOUR TASKS AND RESPONSIBILITIES:</b></p>
<div>
<ul><li>Medical Marketing</li></ul>
</div><ul><li>Provide timely and appropriate medical review of all promotional material as well as challenging promotional activities of competitors where appropriate.</li>
<li>Support development of marketing strategies with respective to competitor innovator and generic brands.</li>
<li>Support BUs in transforming medical data into marketing strategy</li>
<li>Work closely with other members of the medical team (especially the MSLs, if applicable) to support the business</li>
<li>Build up good relationships with customers and TLs</li>
<li>Build strong relationships with internal customers (marketing and sales) and with regional / global Medical Affairs</li>
<li>Provide development project and product training internally to marketing and sales functions and externally to doctors and conduct refresher trainings at appropriate intervals.</li>
<li>Support and educate internal customers in compliance with the Country&rsquo;s Code of Conduct</li>
</ul><div><ul><li>Provide a comprehensive and proactive Medical service that encompasses, as appropriate, including Medical Support, Medical Information and Pharmacovigilance</li></ul>
<ul><li>As Medical/Scientific Advisor, is responsible for overall medical inputs to Integrated Brand Plans of assigned therapeutic areas, provision of scientific expertise, review of promotional materials, thought leader management, speaker development and training.</li></ul>
<ul><li>Takes responsibility for study development programs of the Business units within portfolio (included local studies OS, NIS, IIR). Identifies initiates and completes agreed study development activities in a timely manner, be IIR responsible of local IIR. Takes responsibility for all study development activities that they are running in accordance with all applicable external and internal regulations and guidelines. Play a role as local medical expert for Global Clinical Development by providing inputs for medical queries related to trials; participate in site feasibility.</li></ul>
<ul><li>Respond to all external scientific and medical queries from physicians, regulatory authorities and public alike in an accurate, transparent and convincing manner in order to position Bayer as a credible, trustworthy and professional leader in the industry.</li></ul>
<ul><li>Reviews all local patient support programs and other undertakings of the local organization with potential consequences on PV obligations (e.g. Market Research, Active-Online-Listening programs) to ensure Pharmacovigilance principles are applied in the interaction with patients.</li></ul>
<ul><li>Develops, maintains and strengthens strategic partnership with relevant TLs, societies and associations. Act as medical contact for TL and external Medical experts. In collaboration with local marketing to develop, conduct Advisory Board meetings, Congress and Symposia.</li></ul>
</div>
<p><b>WHO YOU ARE:</b></p>
<ul>
<li>Graduate/ Post graduate degree (MBBS/MD) in life sciences is preferable.</li>
<li>Experience and expertise in relevant TA&rsquo;s or in industry is preferable.</li>
<li>Experience in driving and managing the medical strategy for various brands in the pharmaceutical industry.</li>
<li>Clinical research and trial management experience, and be able to interact authoritatively with key stakeholders and investigators.</li>
<li>Excellent presentation and teaching skills and to represent the company in a professional manner at medical, scientific and public events.</li>
<li>Independent, self-driven, pro-active, extrovert and dynamic</li>
<li>Ability to form relationships quickly and have demonstrable persuasive abilities</li>
<li>Highly effective communicator both orally and in writing; can get ideas across one-on-in, in group settings as well as in presentations</li>
<li>Strong team player and know how to collaborate and engage many stakeholders across a large organization</li>
<li>Innovative and pro-active and has ability of strategic thinking</li>
<li>Results-oriented attitude</li>
<li>Experience in working with MS office in a Windows environment.</li>
</ul>
<p><b>Ever feel burnt out by bureaucracy? Us too. That's why we're changing the way we work- for higher productivity, faster innovation, and better results. We call it Dynamic Shared Ownership (DSO). Learn more about what DSO will mean for you in your new role here</b></p>
<p><b>
https://www.bayer.com/enfstrategyfstrategy</b></p><br>
<p></p>
<p><b>
Bayer does not charge any fees whatsoever for recruitment process. Please do not entertain such demand for payment by any individuals / entities in connection with recruitment with any Bayer Group entity(ies) worldwide under any pretext.</b></p>
<p><b>
Please don&rsquo;t rely upon any unsolicited email from email addresses not ending with domain name &ldquo;bayer.com&rdquo; or job advertisements referring you to an email address that does not end with &ldquo;bayer.com&rdquo;. For checking the authenticity of such emails or advertisement you may approach us at richa.pandey1@bayer.com</b></p><div><div><br>
<div>
</div><br>
<div></div><div><div><b>YOUR APPLICATION</b></div></div><br>
<div></div>
<div>
</div><br>
<div></div><div><div><p>Bayer is an equal opportunity employer that strongly values fairness and respect at work. We welcome applications from all individuals, regardless of race, religion, gender, age, physical characteristics, disability, sexual orientation etc. We are committed to treating all applicants fairly and avoiding discrimination.</p></div><br>
<p></p>
</div><br>
</div></div><div></div><div><div><br>
<div><div><b>Location:</b></div> <div>India : Maharashtra : Thane</div>
</div><br>
<div></div><div><div><b>Division:</b></div> <div>Pharmaceuticals</div>
</div><br>
<div></div><div><div><b>Reference Code:</b></div> <div>855961</div><br>
<div></div>
<div></div>
</div><br>
</div></div><div></div><div><div><br>
<br>
<div><div><b>Contact Us</b></div>
</div><br>
<br>
<div></div><div><div>+ 022-25311234</div></div></div></div></div>

Medical Advisor

Devomech Solutions Pvt. Ltd.

<p>Devomech Solutions and PharmaTech Consult are two growing and passion-driven companies. Devomech Solutions is an innovative firm which is a leading engineering services provider specializing in engineering services, IoT development, electronics design, mechanical design, and firmware development. PharmaTech Consult is a relatively young company based in Denmark, which provides quality medical consultancy/ medical affairs services for pharmaceutical companies.</p><p><b>Responsibilities:</b></p><p>This critical role marks our expansion into services for pharmaceutical companies. Your main tasks include, but are not limited to:</p><ul><li>Learn and adapt to various products and disease areas quickly</li><li>Develop medical communication slide decks for clients.</li><li>Provide medical expertise for various projects.</li><li>Proof-reading and quality control of various client materials.</li><li>Literature review and summarizing key take aways of the articles</li><li>Stay updated on therapy area knowledge.</li><li>Respond to scientific/medical support requests.</li><li>Write abstract and scientific publications</li><li>Develop content for promotional/non-promotional videos</li></ul><p><b>Requirements:</b></p><ul><li>Advanced degree in pharmacy, biology or medicine</li><li>Pharmaceutical industry/ Medical Affairs experience is preferred but not mandatory</li><li>Fluent in English (written and spoken)</li><li>Effective oral and written communication (power point skills are a must-have)</li><li>Good analytical and numerical skills</li><li>Flexibility and agility to deliver results with sense of responsibility</li></ul><p><b>Your team:</b></p><p>You will be part of the Devomech team (based in Islamabad) but will work closely and report to Dr. Samra Sardar, Managing Director of PharmaTech Consult. You will be mentored and exposed to international working standards.</p><p><b>Contact us to apply</b></p><p>Please send your resume or CV and cover letter mentioning why this position has your interest to hiring manager at <b>samrasardar@gmail.com</b>. Even if you don&rsquo;t fulfill all criteria, we would like to hear from you.</p><p><b>What we offer</b></p><ul><li>USD pegged salary</li><li>Performance related annual bonus</li><li>Medical Insurance</li><li>Provident Fund</li><li>Paid Leaves</li><li>Accommodation for out of station employees (only for males)</li><li>Annual increase in salary</li><li>Personal Development</li></ul><p>Job Type: Full-time</p><p>Pay: Rs70,000.00 - Rs80,000.00 per month</p><p>Application Question(s):</p><ul><li>Will you be able to commute G16/3 Islamabad for job?</li></ul><p>Work Location: In person</p>

Medical Writer

TeleDocs Consulting

<p>The MSL will serve as the scientific and clinical bridge between TeleDocs Consulting, healthcare professionals (HCPs), and pharmacy partners nationwide. The role is responsible for providing high-quality medical and product education supporting evidence-based prescribing, and ensuring appropriate use of products within therapeutic guidelines.</p><p><strong><em>Key Responsibilities</em></strong></p><p><strong>Scientific & Clinical Education</strong></p><p>- Deliver product education to practitioners and pharmacies.</p><p>- Present practitioner information at workshops and events</p><p>- Assist pharmacists to register and use the B2B ordering portal</p><p><strong>Stakeholder Engagement</strong></p><p>- Build relationships with HCPs and pharmacies</p><p>- Act as the primary resource for product-related queries</p><p>- Support clinicians in integrating new treatments into prescribing software</p><p><strong>Medical Affairs & Compliance</strong></p><p>- Ensure compliance with Australian regulatory standards</p><p>- Document and track all interactions</p><p>- Provide field feedback to leadership</p><p><strong>Cross-Functional Support</strong></p><p>- Collaborate with commercial, regulatory, and distribution teams</p><p>- Assist in practitioner and pharmacy resource development</p><p><strong>Qualifications & Experience</strong></p><p>- Tertiary qualifications in Pharmacy, Medicine, Biomedical Science, or related field (desirable)</p><p>- 2-3 years' experience in MSL, medical affairs, clinical educator role or similar</p><p>- Knowledge of pharmaceutical/nutraceutical lifecycles</p><p>- Experience in alternative healthcare, women's health, men's health, gut health or novel therapeutics (advantageous)</p><p>- Ability to engage and educate healthcare professionals</p><p>- Understanding of TGA regulations and unapproved medicine pathways</p><p><strong>Skills & Attributes</strong></p><p>- Excellent presentation and communication skills</p><p>- Ability to interpret and present data</p><p>- Strong organisational and project management skills</p><p>- Proactive, adaptable and self-motivated</p><p>TeleDocs Consulting is creating a pool of experienced MSL's to work in their own geographical location and collectively build networks nationwide. MSL's will work strategically together to grow the capabilities of the business to increase service offerings to clients. </p><p>TeleDocs Consulting will offer short-term and long-term contracts to the MSL based on their availability, knowledge and experience to match the contract requirements.</p><p>TeleDocs Clinic & Consulting provides a portfolio of services to clients in the pharmaceutical sector. The MSL team form a key part of the collaboration between proven digital health solutions and TeleDocs Clinic services to provide a strategic approach to deliver contract outcomes.</p><p>Apply for this role if this sounds like you and we will review your application.</p><p>Job Type: Full-time</p><p>Benefits:</p><ul><li><p>Professional development assistance</p></li><li><p>Work from home</p></li></ul>

Medical Science Liaison

Abbott

<div><p>MAIN PURPOSE OF ROLE</p><p>
Experienced professional individual contributor that works under limited supervision.</p><p>
Applies subject matter knowledge in the area of Medical Affairs.</p><p>
Requires capacity to apply skills/knowledge within the context of specific needs or requirements.</p><p></p><p>
MAIN RESPONSIBILITIES</p><ul><li>As the Experienced professional in the Medical Affairs Sub-Function, possesses well developed skills</li></ul><p>
in overseeing the direction, planning, execution, clinical trials/research and the data collection</p><p>
activities.</p><ul><li>Contributes to implementation of clinical protocols, and facilitates completion of final reports.</li><li>Recruits clinical investigators and negotiates study design and costs.</li><li>Responsible for directing human clinical trials, phases III &amp; IV for company products under</li></ul><p>
development.</p><ul><li>Participates in adverse event reporting and safety responsibilities monitoring.</li><li>Coordinates and provides reporting information for reports submitted to the regulatory agencies.</li><li>Monitors adherence to protocols and determines study completion.</li></ul><p>
Coordinates and oversees investigator initiations and group studies.</p><ul><li>May participate in adverse event reporting and safety responsibilities monitoring.</li><li>May act as consultant/liaison with other corporations when working under licensing agreements.</li></ul><p></p><p>
QUALIFICATIONS</p><p>
Education</p><p>
Education Level Major/Field of Study or Equivalent</p><p>
Associates Degree (&plusmn; 13</p><p>
years)</p><p>
Experience/Background</p><p>
Experience Experience Details</p><p>
Minimum 1 year</p></div>

Regional Medical Advisor

Boehringer Ingelheim

<div>
 <strong>
  Our Company
  <br/>
  <br/>
 </strong>
 At Boehringer Ingelheim we develop breakthrough therapies that improve the lives of both humans and animals. Founded in 1885 and family-owned ever since, Boehringer Ingelheim takes a long-term perspective.
 <br/>
 <br/>
 Now, we are powered by 52,000 employees globally who nurture a diverse, collaborative and inclusive culture. We believe that if we have talented and ambitious people who are passionate about innovation, there is no limit to what we can achieve.
 <br/>
 <br/>
 <strong>
  THE POSITION
  <br/>
  <br/>
 </strong>
 We are looking for an undergraduate student preferably in Medicine, Pharmacy or related fields who is interested in intern position for Medical Affairs.
 <br/>
 <br/>
 <strong>
  Tasks &amp; Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Providing support to the medical affairs department for administrative processes,
  </li>
  <li>
   Contributing medical team as an active member,
  </li>
  <li>
   Taking an active role for initiatives that are ongoing and will be planned across all TAs in the medical department,
  </li>
  <li>
   Preparing and checking project related forms, documentations and mails, submissions of the documentations to the necessary online systems, following up with approvals and filing all documentations in accordance with the rules,
  </li>
  <li>
   Assisting and following up communication and coordination within and between the departments
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Requirements
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Undergraduate (3rd,4th or 5th year) student preferably in Medicine, Pharmacy or related fields,
  </li>
  <li>
   Willingness to Learn and Develop Personal Qualifications,
  </li>
  <li>
   Strong verbal and written communication skills both in Turkish&amp;English,
  </li>
  <li>
   Strong analytical, organization, critical-thinking, problem-solving skills,
  </li>
  <li>
   A strong sense of ownership and accountability,
  </li>
  <li>
   Project Management ability with developed follow-up skills,
  </li>
  <li>
   Ability to work independently and as part of a team,
  </li>
  <li>
   Excellent organizational skills, attention to detail, and the ability to prioritize in a changing environment,
  </li>
  <li>
   Experience in Microsoft Programs like Excel and Power Point is a bonus,
  </li>
  <li>
   Able to work at least 3 days in a week and continue for 6 months
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  WHY BOEHRINGER INGELHEIM?
  <br/>
  <br/>
 </strong>
 With us, you can grow, collaborate, innovate and improve lives.
 <br/>
 <br/>
 We offer challenging work in a respectful and friendly global working environment surrounded by a world of innovation driven mindsets and practices. In addition, learning and development for all employees is key, because your growth is our growth.
 <br/>
 <br/>
 Our Company
 <br/>
 <br/>
 <strong>
  Why Boehringer Ingelheim?
  <br/>
  <br/>
 </strong>
 With us, you can develop your own path in a company with a culture that knows our differences are our strengths - and break new ground in the drive to make millions of lives better.
 <br/>
 <br/>
 Here, your development is our priority. Supporting you to build a career as part of a workplace that is independent, authentic and bold, while tackling challenging work in a respectful and friendly environment where everyone is valued and welcomed.
 <br/>
 <br/>
 Alongside, you have access to programs and groups that ensure your health and wellbeing are looked after - as we make major investments to drive global accessibility to healthcare. By being part of a team that is constantly innovating, you'll be helping to transform lives for generations.
 <br/>
 <br/>
 Want to learn more? Visit https://www.boehringer-ingelheim.com
</div>


Medical Affairs Intern

Guardant Health

<div><b>Company Description</b><p><br>
Guardant Health AMEA is a leading precision oncology company advancing cancer care across Asia, the Middle East, and Africa. We harness cutting-edge liquid biopsy technology, real-world data, and AI-driven insights to support earlier detection, treatment selection, and monitoring of cancer. Our flagship test, Guardant360&reg;, is the first FDA-approved comprehensive liquid biopsy for advanced solid tumors&mdash;marking a major milestone in non-invasive cancer diagnostics. Operating in over 40 countries, we are committed to expanding access to innovative solutions that improve outcomes and transform the standard of care for patients across the region.</p><b><br>
Job Description</b><p><b><br>
Position Summary:</b></p><ul><li>
The primary role of the Medical lead is to facilitate the generation of relevant medical evidence to support Guardant AMEA products and to instil confidence among healthcare providers, payers, and internal stakeholders regarding the use of Guardant AMEA products in the MENA region.</li><li>
The Medical lead will identify clinical evidence gaps and identify and support opportunities for internal and external clinical research of Guardant AMEA products that are aligned with corporate goals and adhere to local compliance standards in the assigned countries. This will also include working and supporting publications of GH AMEA supported evidence generation activities.</li><li>
The Medical lead will review and coordinate proposals for investigator-sponsored research from disease area experts within the region, present such proposals for review at internal meetings, and facilitate operational processes for the successful completion of approved projects, including when appropriate, interpretation and review of scientific content (abstracts, posters, presentations, manuscripts) for public dissemination by the investigators.</li><li>
Medical lead is responsible for developing and executing the plan for educating health care providers, including leading disease area experts, by creating, updating, and sharing the most current educational materials supporting the clinical value of our products. Medical Lead will also engage with public health bodies to champion the usage and utilization of GH platforms and assays.</li><li>
Medical lead is responsible for prioritization of leading experts and clinical centers as it relates to the education plan; this includes identifying influential content experts, leaders of scientific committees within academic research groups, and members of relevant treatment and diagnostic guideline committees in the assigned countries.</li><li>
Medical lead will be effective at translating data from research projects and disseminating key information through publications, presentations at national or regional meetings, CME events, and other educational activities.</li><li>
When requested by Client Services, the Medical lead will support healthcare providers regarding the appropriate interpretation of clinical reports generated as part of Guardant AMEA products.</li><li>
Medical lead will provide medical educational support to internal Guardant AMEA teams and, as needed, medical support for regulatory, reimbursement, and business development activities in the assigned countries to meet corporate goals.</li><li>
Medical Lead will lead and support the medical activities for distributors of GH AMEA products in MENA region. This will include strategic oversight of key activities and assay and disease state trainings and expertise.</li></ul><p></p><b><br>
Qualifications</b><br>
<ul><li>
MD or MBBS or PhD or life science</li><li>
Clinical expertise or related experience in relevant specialties is highly desirable.</li><li>
Minimum of 2 years of experience in Oncology Medical Affairs</li><li>
Experience working with experts at academic medical centers to build consensus around</li><li>
new products and/or services.</li><li>
Prior experience in Medical Affairs and/or in the introduction of a novel clinical product</li><li>
Willingness to work at all levels and cross-functionally to support team goals.</li><li>
Strong problem-solving skills, good attention to detail, time management, and personal</li><li>
initiative.</li><li>
Excellent interpersonal, verbal and written English communication skills.</li></ul><br>
<b>
Additional Information</b><p><b><br>
Work Environment:</b></p><ul><li>
Travel required, occasionally up to 5 days within a week, to meet with experts, and attend physician education talks and conference, including specialty society scientific meetings (will require some weekend work).</li><li>
Must be physically able to handle extensive travel in a vehicle, plane or other modes of public transport.</li><li>
Requires the ability to focus on multiple tasks simultaneously, and work in a high-paced, high-energy environment.</li></ul></div>

Medical Lead, MENA

Getz Pharma

<div>
 <p>
  <strong>
   <u>
    Position Summary:
   </u>
  </strong>
 </p>
 <p>
  Drive pipeline planning &amp; development activities to consistently replenish Getz Pharma&rsquo;s generic and biosimilar pipeline with new products in Pakistan and International markets, targeting early access for patients. Perform &amp; execute the ideation, lead generation, holistic evaluation and other project management activities for introduction &amp; induction of new products &amp; therapies, new segments, new facilities/technologies and business partnerships.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   <u>
    Requirements:
   </u>
  </strong>
 </p>
 <ul>
  <li>
   PharmD/MBBS, MBA preferable but not mandatory
  </li>
  <li>
   Candidate should have a strong business as well as scientific acumen
  </li>
  <li>
   Should possess a flair for Pharmacology
  </li>
  <li>
   Innovative professional with interest in novel therapies
  </li>
  <li>
   4-6 yrs of overall experience with current experience in Business development function of reputed pharmaceutical industry is desirable. Prior work experience in Medical Affairs function of pharma industry or a large tertiary care hospital will be encouraged.
  </li>
 </ul>
</div>


Assistant Manager Business Development

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