Clinical Development Physician CLIN BIOSCIENCES

About CLIN BIOSCIENCES

Job Description

The Clinical Development Physician plays a pivotal role in designing, reviewing, and leading clinical development programs in line with global regulatory standards. The role requires strong medical and scientific expertise to support the planning, execution, and monitoring of clinical trials across different phases, with a focus on safety, efficacy, and compliance.

Roles and Responsibilities;

• Design and provide medical oversight for clinical trials (Phase IIV).

• Review and approve protocols, CRFs, ICFs, Investigator Brochures, and CSRs.

• Serve as the clinical point of contact for cross-functional teams including regulatory, pharmacovigilance, biostatistics, and medical writing.

• Monitor trial safety data, participate in DSMB meetings, and contribute to signal detection and risk management planning.

• Actively contribute to regulatory submissions, including CTAs, INDs, NDAs, and MAAs.

• Represent the company in investigator meetings, advisory boards, and scientific conferences.

• Provide medical expertise in therapeutic areas such as oncology, cardiology, CNS, or rare diseases, as per company portfolio.

Eligibility / Qualifications:

• MBBS / MD / DO or equivalent medical degree.

• Prior experience in CRO, pharma, or regulatory consulting is preferred.

• Clinical research certifications (e.g., ACRP, DIA, ICH-GCP) are an advantage.

• Familiarity with EMA, FDA, and GCC regulatory requirements is a strong plus.

Interested to apply can share you CV in Whatsapp/Call to 9342735755