• Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiological Practices (GPP) and protocol compliance. • Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions; immediately communicates/escalates serious issues to the project team and with guidance develops action plans. • Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes. • Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient, as required/appropriate. • Demonstrates diligence in protecting the confidentiality of each subject/patient. • Assesses factors that might affect subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. • Conducts Source Document Review of appropriate site source documents and medical records. • Verifies required clinical data entered in the case report form (CRF) is accurate and complete. • Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines. • Verifies site compliance with electronic data capture requirements. • Ensures the investigator/physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations. • Supports subject/patient recruitment, retention and awareness strategies. • Must be able to quickly adapt, with the oversight of the Lead CRA, to changing priorities to achieve goals / targets.

Role Description As a Research Associate with the Numerator Pre-field Team, you will be a vital member of our team, focusing on impeccable quality deliverables for your assigned projects. Your responsibilities will include: - Building surveys in our programming platforms (Qualtrics and/or Alchemer) - Deployment and soft-launch of the survey using our proprietary tool (Atlas) - Quota and field management - Quality checking data in the field - Making report links - Drafting tab plans for the final crosstabs of the project You will be the primary point of contact for your assigned survey projects with U.S. team members. Shift Timings: Rotating General Shift: 11:00 a.m.–8:00 p.m. IST Late Evening Shift: 5:30 PM IST–2:30 AM IST (5 days in a month) Qualifications - Bachelor's degree (any field) with a passion for marketing, research, and account management or growth - Proficient in Excel and PowerPoint (or equivalent) - Excellent oral and written communication skills - Self-confidence coupled with strong presentation skills - Strong attention to detail - Experience working with large data sets is a plus - Experience in Python and/or JavaScript is a plus - A logical mindset can handle intricate logic Company Description

Role Description The Therapeutic Area Lead is responsible for supporting the strategic development of PSI's core indications and serves as a core support function. As PSI continues to expand its Gastroenterology portfolio, we are seeking a Therapeutic Area Lead with expertise in Inflammatory Bowel Disease (IBD), particularly Ulcerative Colitis and Crohn's Disease, to serve as a scientific and strategic subject matter expert across the organization. This highly visible role partners with Business Development, Proposal Development, Clinical Operations, and Study Teams to support growth initiatives, client engagement, therapeutic strategy, and operational excellence within the GI therapeutic area. The successful candidate will help shape PSI's long-term GI strategy while serving as a trusted advisor to both internal stakeholders and external clients. Responsibilities - Supports indication-specific strategy planning and implementation across the assigned therapeutic area. - Attends conferences in the therapeutic area and reviews supporting literature. - Compiles datasets, metrics, lessons learned, and performance indices on core strategic capabilities and key studies within the given therapeutic area. - Supports project teams within assigned indications to advise on therapeutic strategy and study-specific mitigation strategies. - Supports the evaluation and selection of investigative sites. - Participates in Investigator Meetings and key team meetings. - Performs protocol analysis and escalates risks to senior management. - Reviews essential study documents and technical manuals. - Performs background research on epidemiology and other aspects of the given indication. - Supports client engagement and business development from a therapeutic area perspective. - Participates in proposal development and bid defense meeting preparations. - Supports PSI's KOL networks within the assigned therapeutic area. Qualifications - College or university degree in Life Sciences; advanced scientific degree or clinical degree is a plus. - At least 6 years of experience in Gastroenterology within academia, clinical practice, laboratory, biotechnology, pharmaceutical, CRO, or clinical research environments. - Demonstrated experience within Inflammatory Bowel Disease, particularly Ulcerative Colitis and Crohn's Disease. - Strong scientific and analytical capabilities. - Ability to review and interpret clinical protocols and study documentation. - Strong written and verbal communication skills. - Ability to build effective relationships with internal and external stakeholders. - Ability to work effectively across multiple functional teams. - Proficiency in standard MS Office applications. Additional Information Join a growing therapeutic strategy function and play a key role in shaping PSI's Gastroenterology portfolio. This is a unique opportunity to combine scientific expertise, strategic thinking, and business impact while collaborating with sponsors, investigators, and cross-functional teams across the organization.

• Desk research: Reviewing and collecting information from secondary sources • Storechecks: Visiting retail stores and points of sales to record product information • Trade interviews: Conducting face to face or phone interviews with different key players of the value chain: manufacturers, suppliers, distributors • Data building: Collecting and manipulating data points in order to build market sizes, brand participation, etc. • Analysis: Analysing quantitative and qualitative data / information - Hypothesis testing