Careers
Join our team and be part of a dynamic, forward-thinking organization dedicated to ensuring patient safety, regulatory compliance, and innovative pharmacovigilance solutions
JOIN OUR TEAM
Interested in Working for CliniResource ?
CliniResource is a leader in providing clinical research, pharmacovigilance, and regulatory affairs services to the biotech and pharmaceutical industries. We are a passionate team dedicated to helping our clients bring innovative healthcare solutions to market.
Look at the available open positions below or e-mail your full resume in english to Jobs@CliniResource.com
Where Innovation Meets Opportunity in Healthcare
Join our passionate team and accelerate advancements in patient care through clinical research and development. We invest in your growth with learning programs, mentorship, and challenging projects. Collaborate with a talented team in a dynamic environment that fosters innovation. We offer competitive salaries, bonuses, and a comprehensive benefits package to support your well-being. Join us and make a real impact in healthcare Industry at CliniResource.
Why Choose CliniResource?
Make a Difference:
Be part of a team that is accelerating advancements in healthcare. At CliniResource, your work directly contributes to getting new treatments, medications, and healthcare technologies to the people who need them most. You’ll be involved in projects that:
- Speed Up Clinical Trials: By working efficiently and accurately, you’ll help ensure new drugs and treatments get tested and approved faster. This means patients can access potentially lifesaving therapies sooner.
- Improve Patient Safety: Your work in pharmacovigilance helps identify and address potential risks associated with medications. This contributes to creating safer and more effective treatments for everyone.
- Advance Medical Knowledge: Your role in regulatory affairs helps ensure that new healthcare solutions meet the highest safety and efficacy standards. This contributes to the overall progress of medical science.
By joining CliniResource, you’ll be at the forefront, playing a crucial role in bringing the future of healthcare to reality.
Growth Opportunities:
We invest in our employees’ professional development. At CliniResource, we understand that our employees are our greatest asset. That’s why we’re committed to investing in your professional development and helping you reach your full potential. Here’s what you can expect:
- Learning & Development Programs: We offer a variety of training programs, workshops, and conferences to help you develop new skills and stay current in the ever-evolving healthcare industry.
- Mentorship & Coaching: We connect you with experienced mentors who can provide guidance, support, and career advice.
- Challenging Projects & Responsibilities: We believe in providing you with opportunities to stretch your skills and take on new challenges. This will help you broaden your experience and prepare for future advancements in your career.
- Career Development Planning: We work with you to identify your career goals and create a development plan to help you achieve them.
At CliniResource, we’re not just focused on your current role; we’re invested in your long-term career success.
Dynamic Work Environment:
Collaborate with a talented and experienced team. At Clini Resource, you won’t be working in a silo. You’ll be part of a dynamic and collaborative environment where you can:
- Learn from the Best: Our team is comprised of highly skilled and experienced professionals across various healthcare research and regulatory disciplines. You’ll have the opportunity to work alongside mentors who can share their knowledge and expertise.
- Cross-Functional Collaboration: We encourage collaboration across departments. This allows you to gain a broader understanding of the healthcare research and development process, and how your role contributes to the bigger picture.
- Open Communication & Feedback: We foster a culture of open communication and feedback. You’ll be encouraged to share your ideas, ask questions, and learn from your colleagues.
- Innovation is Encouraged: We value innovative thinking and creative problem-solving. You’ll have the opportunity to contribute your ideas and work on projects that push the boundaries of healthcare advancement.
This dynamic environment will not only challenge you to grow professionally but also create a sense of collegiality and shared purpose within the team.
Competitive Benefits:
At CliniResource, we understand that a rewarding career goes beyond just a paycheck. That’s why we offer a comprehensive benefits package designed to support your financial security, well-being, and professional development:
Competitive Salaries: We offer competitive salaries that are benchmarked against the industry standard and reflect your skills and experience.
Performance-Based Bonuses: We recognize and reward your hard work and contributions to our success through performance-based bonus programs.
- Paid Time Off: We believe in the importance of work-life balance and offer generous paid time off benefits, including vacation days, sick leave, and personal days.
By offering a competitive benefits package, we want to show our appreciation for your talent and dedication. We’re committed to creating a work environment that fosters your personal and professional well-being.
We are always looking for talented individuals to join our team. If you are passionate about the healthcare industry and have the skills and experience to contribute to our success, we encourage you to submit your resume and cover letter to Jobs@CliniResource.com even if there are no open positions listed.
Build a Rewarding Career at CliniResource
We believe in creating a positive and supportive work environment where our employees can thrive. If you are looking for a challenging and rewarding career in the healthcare industry, we encourage you to explore the opportunities at CliniResource.
Company Values
By living our values, we create a meaningful and rewarding work environment where our team can thrive and contribute to groundbreaking advancements in healthcare. Join us and be part of something bigger!
Patient Focus
We are dedicated to putting the well-being of patients at the forefront of our work. Every decision we make is driven by the potential impact on patient care.
Scientific Excellence
We uphold the highest standards of scientific rigor and integrity in our clinical research, pharmacovigilance, and regulatory affairs services.
Collaboration
We believe in the power of teamwork and foster a collaborative environment where open communication, knowledge sharing, and mutual respect are paramount.
Innovation
We are committed to continuous learning, embracing new ideas, and pushing the boundaries of healthcare research to deliver groundbreaking solutions.
Integrity & Ethics
We act with honesty, transparency, and the highest ethical standards in all our interactions with clients, colleagues, and the healthcare industry.
Client Focus
We build strong partnerships with our clients, understanding their unique needs and tailoring our services to achieve their goals.
Quality & Excellence
We invest in ongoing training and development for our team, ensuring they possess the expertise to deliver the highest quality work.
Openness
We encourage open communication across departments and foster a culture of teamwork where everyone's voice is heard.
Research & Development
We support ongoing research and development initiatives, exploring new technologies and methodologies to advance healthcare research.
Good Practices
We adhere to the good pharmacovigilance practices & guidelines in all our work for our clients and the industry.
Current Openings
Medical Reviewer, ICSR
About the job
CliniResource is a global full-service CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative “one-team” culture. We are looking for a dynamic person to join our in-house team as a Medical Reviewer on a permanent basis. You will work on projects from our varied client base, ranging from small to big pharmaceutical, biotechnology, medical device and consumer health companies.
Join our team: you can be part of making a difference in peoples’ lives and experience a fulfilling and rewarding career!
Main Job Tasks and Responsibilities:
- Awareness and understanding of relevant GVP modules.
- Perform medical review of non-serious and serious ICSRs with emphasis on seriousness, expectedness, causality & narrative, etc. without missing on quality & compliance.
- Experience of medical review of ICSRs received from sources such as Spontaneous, Literature, Regulatory Authority, Solicited and Clinical trials.
- Experience across multiple therapeutic areas such as Oncology, Respiratory, Immunology, Neuroscience, Rare diseases, etc.
- Support triage of cases and determine seriousness and relatedness across products as assigned.
- Review and verify appropriate selection of adverse events from source documents, assign appropriate MedDRA code, assess labelling and review narrative.
- Acquire and maintain current knowledge of product portfolio and safety profiles for products across therapeutic areas.
- Involve in process improvement activities such as implementation of quality control process.
- Provide medical guidance and expert opinion on the cases to the data entry associates and quality reviewers to help resolve queries.
- Identify and resolve case issues, coordinate with client therapeutic teams and within functional team and manage as appropriate.
- Maintain Pharmacovigilance expertise and understanding of international safety regulations and guidelines.
- Responsible for completing the medical review activities in the safety database within the stipulated time to comply with service level agreements and regulatory timelines.
- Provide timely feedback to case processors on the errors/discrepancies noted.
- Assist in training/mentoring of other case processing/medical review personnel as necessitated.
- Adapt to different client case processing conventions and multi-task as per business needs.
- Perform ad-hoc tasks as advised by the team lead/manager with quality and compliance as per project requirement.
- Participate in organizational activities to meet objectives suitable for the role/area of expertise.
Education, Experience and Skills:
- Should be a MBBS/MD with 2- 4 years of experience as Medical Reviewer for ICSRs.
- Must possess thorough knowledge of ICH-GCP, relevant GVP module, 21 CFR guidelines and other regulatory requirements.
- Training and mentoring skill (GVP concepts & medical aspects such as disease condition, product portfolio, etc).
- Must have hands on experience with MS Office applications (Outlook, Excel, Word, PowerPoint, etc.).
The Application Process
Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.
Job Features
About the job CliniResource is a global full-service CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative “one-team” cultur...View more
Pharmacovigilance Services Specialist
What are we looking for?
Key Abilities:
- Ability to manage multiple stakeholders
- Ability to perform under pressure
- Collaboration and interpersonal skills
- Prioritisation of workload
- Agility for quick learning
Roles and Responsibilities:
- Perform analysis and solve moderately complex problems
- Create new solutions by leveraging and adapting existing methods and procedures
- Understand strategic direction set by senior management related to team goals
- Primary interaction with direct supervisor
- May interact with peers and management levels at client or within CliniResource
- Receive guidance when determining methods and procedures for new assignments
- Make decisions that impact the team
- Manage small teams or work efforts (in an individual contributor role)
- Potential requirement to work in rotational shifts
Job Features
What are we looking for? Key Abilities: Roles and Responsibilities: