About Clinforge Clinforge Clinical Research Solutions Pvt. Ltd. is a growing Contract Research Organization (CRO) dedicated to delivering high-quality services in clinical research, regulatory affairs, pharmacovigilance, and scientific/medical writing . Our mission is to bridge science and communication by transforming complex research into impactful knowledge. Key Responsibilities Develop, write, and edit scientific manuscripts, review articles, case studies, and conference abstracts/posters . Prepare regulatory and clinical documents (clinical study reports, investigator brochures, patient information leaflets, regulatory dossiers). Create medical communication materials including slide decks, CME content, and white papers for healthcare professionals. Collaborate with researchers, clinicians, and regulatory teams to ensure accuracy, consistency, and compliance with journal/regulatory requirements. Conduct literature reviews and ensure referencing accuracy (PubMed, Scopus, etc.). Ensure documents follow ICMJE, GCP, CONSORT, and journal-specific guidelines . Maintain high standards of clarity, accuracy, and scientific integrity . Qualifications & Skills Master’s or PhD in Life Sciences / Pharmacy / Biotechnology / Clinical Research . 1–3 years of experience in scientific or medical writing (Fresher with strong writing skills may be considered). Strong command of English language, grammar, and scientific terminology . Familiarity with journal submission processes and reference management software (EndNote, Mendeley, Zotero). Knowledge of regulatory writing (CSR, CTD/eCTD modules) will be an added advantage. Excellent communication, attention to detail, and ability to meet deadlines.
You will be responsible for the following key tasks: - Develop, write, and edit various scientific manuscripts, review articles, case studies, and conference abstracts/posters. - Prepare regulatory and clinical documents such as clinical study reports, investigator brochures, patient information leaflets, and regulatory dossiers. - Create medical communication materials including slide decks, CME content, and white papers tailored for healthcare professionals. - Collaborate effectively with researchers, clinicians, and regulatory teams to ensure accuracy, consistency, and compliance with journal/regulatory requirements. - Conduct thorough literature reviews and ensure precise referencing using platforms like PubMed and Scopus. - Ensure that all documents adhere to ICMJE, GCP, CONSORT, and other journal-specific guidelines. - Maintain exceptionally high standards of clarity, accuracy, and scientific integrity. Your qualifications and skills should include: - A Masters or PhD in Life Sciences, Pharmacy, Biotechnology, or Clinical Research. - At least 3 years of experience in scientific or medical writing; however, exceptional freshers with strong writing abilities may also be considered. - Proficient command of the English language, grammar, and scientific terminology. - Familiarity with journal submission processes and reference management software such as EndNote, Mendeley, and Zotero. - Knowledge of regulatory writing, including CSR and CTD/eCTD modules, would be a valuable asset. - Excellent communication skills, keen attention to detail, and the ability to consistently meet deadlines.,
We are a growing organization with two specialized divisions – Clinforge Clinical Research Solutions (our CRO arm) and CPA Institute of Pharmaceuticals & Life Sciences (our academy arm). We are looking for a dynamic professional who can manage HR responsibilities for Clinforge while also leading training & placement activities at CPA Institute. Job Responsibilities (Split by Division) At Clinforge (CRO arm) – HR Responsibilities • End-to-end recruitment (medical writers, CRAs, interns, corporate staff). • Employee onboarding, payroll, and compliance. • Employee engagement & performance management. • Draft & implement HR policies. At CPA Institute (Academy arm) – Placement Responsibilities • Build strong industry connections (pharma, biotech, CROs, hospitals). • Organize campus recruitment drives, career fairs, and guest sessions. • Guide students in CV building, interview prep, and career readiness. • Track and maintain placement records & alumni relations.
As a dynamic professional at our organization, you will be responsible for managing HR responsibilities for Clinforge Clinical Research Solutions (our CRO arm) while also leading training & placement activities at CPA Institute of Pharmaceuticals & Life Sciences (our academy arm). Role Overview: You will play a key role in handling HR responsibilities at Clinforge, including end-to-end recruitment for various positions such as medical writers, CRAs, interns, and corporate staff. Additionally, you will focus on employee engagement, performance management, and the drafting and implementation of HR policies. Key Responsibilities: - End-to-end recruitment for medical writers, CRAs, interns, and corporate staff. - Employee engagement and performance management. - Drafting and implementing HR policies. At CPA Institute, you will be responsible for placement-related activities, including building strong industry connections with pharma, biotech, CROs, and hospitals. You will organize campus recruitment drives, career fairs, and guest sessions. Moreover, you will guide students in CV building, interview preparation, and career readiness, while also tracking and maintaining placement records and alumni relations. Qualifications Required: - Bachelor's degree in Human Resources, Business Administration, or a related field. - Prior experience in HR management and/or training and placement activities in the pharmaceutical or life sciences industry would be advantageous. (Note: No additional details of the company were provided in the job description),
Visit doctors and healthcare professionals to present and support slide deck projects. • Engage with pharmaceutical companies to promote and secure scientific & medical writing projects. • Visit pharmacy and medical colleges for academic collaborations, training opportunities, and project discussions. • Assist in organizing and coordinating CMEs (Continuing Medical Education programs), workshops, and awareness sessions with healthcare stakeholders. • Build and maintain long-term professional relationships with doctors, institutions, and pharma clients. • Collect feedback, prepare visit reports, and contribute to business development strategies. Desired Candidate Profile: • Minimum 1 year of experience as a Medical Representative or in a similar field role within the pharmaceutical/healthcare industry. • Strong communication, presentation, and relationship-building skills. • Ability to travel extensively within assigned territory. • Self-motivated, goal-oriented, and comfortable with target-based performance.
Company Description Clinforge Clinical Research Solutions Pvt. Ltd. is an emerging Contract Research Organization (CRO) dedicated to advancing excellence in scientific writing, regulatory documentation, and clinical research support services. Headquartered in Lucknow, India, Clinforge operates at the intersection of education, research, and regulatory compliance , serving as a bridge between academic innovation and industry implementation. With a focus on quality, ethics, and precision, Clinforge provides customized solutions to pharmaceutical, biotechnology, and academic partners seeking expertise in medical and scientific communication, clinical data documentation, and regulatory submissions. We suggest you enter details here. Role Description Regulatory Documentation Standards · Align all medical/scientific writing with ICMJE, GPP3, and ICH E6 (R2) . · Create internal SOPs for Manuscript Writing, Literature Review, and Publication Ethics. · Set up templates for CSR, IB, and CTD documentation (for future regulatory writing projects). · Publication & Compliance Oversight · Ensure Clinforge’s Journal of Drug Development & Clinical Research (JDDCR) follows COPE guidelines. · Support ISSN registration, peer-review documentation, and indexing compliance. · Institutional Ethics & Audit Readiness · Prepare Clinforge for future CRO licensing by documenting SOPs and quality standards. · Liaise with consultants for registration under CDSCO / Institutional Bioethics Committee in future phase. AICTE/PCI/UGC Alignment · Study guidelines for Skill Development Courses , Value-Added Programs , and Vocational Education . · Draft frameworks for credit-based certification courses as per AICTE Model Curriculum for Pharmacy Education . · Prepare documents for MoUs, add-on courses, and short-term program approvals. · NAAC Compliance · Design documentation templates for colleges (Attendance, Feedback, Outcome Mapping). · Create a “CPA Compliance Handbook” that partner colleges can use during NAAC visits. · Map each CPA course with Learning Outcomes required under NAAC/NBA. Qualifications Experience in Regulatory Documentation and Dossier Preparation In-depth understanding of Regulatory Requirements and Regulatory Compliance Proven experience in Regulatory Affairs Excellent written and verbal communication skills Detail-oriented and highly organized Ability to work independently and collaboratively Advanced degree in a relevant field (e.g., life sciences, pharmacy, law) is a plus Experience in the healthcare or pharmaceutical industry
Company Description We suggest you enter details here. Role Description The Scientific Writer will be responsible for producing high-quality, accurate, and concise scientific documents. This includes developing and editing manuscripts, research articles, and medical content based on scientific data. The role involves conducting in-depth research, collaborating with other professionals, and ensuring scientific accuracy and compliance with guidelines. This is a full-time, on-site role based in Lucknow. Qualifications Strong skills in Scientific Writing, Medical Writing, and general Writing Proficiency in conducting detailed Research and synthesizing information Excellent Communication skills, both written and verbal Attention to detail and the ability to handle complex scientific material Relevant educational background in science, healthcare, or a related field (advanced degrees preferred) Familiarity with industry-specific standards, technologies, and formatting is an added advantage