Medical Affairs Specialist
for section headings: About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. Only include sections that have real specific content. Must not repeat job title as heading. Must not include Job ID etc. Remove boilerplate like EEO, etc. Must preserve all substantive info.
We need to parse the posting.
Key info:
- Primary Talent Partners has a new contract opening for a Medical Affairs Specialist to join our pharmaceutical client in North Wales, PA. This is a 12-month contract to start with the potential for extensions. Pay: $65.00 - $85.00/hr; W2 contract, no PTO, no Benefits. ACA-compliant supplemental package available for enrollment. Candidates must be legally authorized to work in the United States and must be able to sit on Primary Talent Partners W2 without sponsorship. Hybrid schedule of three flexible onsite days per week.
- Description Responsibilities: The Global Medical Information (GMI) Senior Specialist is an entry-level headquarters-based role within Global Medical & Scientific Affairs, who is responsible for US and global core functions of the GMI group: Medical Information, which includes handling of all US healthcare professional (HCP) inquiries and escalated complex global HCP inquiries as well as generating insights and analysis. Medical Review of promotional and non-promotional scientific materials. Compendia and Pathways Submissions. The responsibilities and activities of the Senior Specialist are focused on the US and global core functions of GMI with guidance from senior GMI colleagues.
- Key Skills: Advanced scientific or clinical degree, preferably a PharmD or PhD. Medical review expertise, the primary need for this position. Medical information experience. Strong knowledge of clinical trials. Excellent written and verbal communication skills. Strong organization and prioritization skills. Oncology knowledge preferred. At least two years of relevant experience is required. Pharmaceutical, CRO, medical communications agency, fellowship, internship, and co-op experience may be considered.
- Qualifications: Required Education Advanced degree (PharmD, PhD, MS or equivalent) that is relevant to the requirements of the position. Required Experience and Skills: Some work experience in Medical Information and/or Medical/Scientific Review of promotional materials in the biotech/pharmaceutical or healthcare environment. Strong knowledge of clinical trial methodology, statistical concepts, and evaluation and interpretation of complex scientific literature. Excellent interpersonal and communication skills. Organizational and prioritization skills. Some knowledge and therapeutic area experience in Oncology. Preferred Experience and Skills: 2 years of medical information or medical/scientific review or relevant biotech/pharmaceutical experience. Deep experience working in Medical Information and/or prior biotech/pharmaceutical industry experience. Advanced knowledge and therapeutic area experience in Oncology. Strong working knowledge of Microsoft Office Suite and systems for Medical Information and Promotional Review. Negotiation skills for interaction with cross-functional teams.
- Note: Hybrid Position is in Upper Gwynedd, PA- requires 3 days in the office.
- Also mention: Pay: $65.00 - $85.00/hr; W2 contract, no PTO, no Benefits. ACA-compliant supplemental package available for enrollment.
- Hybrid schedule of three flexible onsite days per week.
- Must be legally authorized to work in US, must be able to sit on Primary Talent Partners W2 without sponsorship.
We need sections: About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule.
We need to decide what goes where.
- About the role: could include description of role, location, contract length, etc. The posting says: "Primary Talent Partners has a new contract opening for a Medical Affairs Specialist to join our pharmaceutical client in North Wales, PA. This is a 12-month contract to start with the potential for extensions." Also mention hybrid schedule? Might be schedule.
- Responsibilities: list bullet points: handling US and global HCP inquiries, generating insights and analysis, medical review of promotional and non-promotional scientific materials, compendia and pathways submissions.
- Requirements: maybe required education and experience: advanced degree (PharmD, PhD, MS), some work experience in medical information or medical/scientific review, strong knowledge of clinical trial methodology, etc. Also must be legally authorized to work in US, able to sit on W2 without sponsorship.
- Qualifications: maybe the "Preferred Experience and Skills" and "Required Experience and Skills"? But we already used some in Requirements. Could separate: Requirements = required education/experience; Qualifications = preferred qualifications.
- Skills: list key skills: advanced scientific/clinical degree, medical review expertise, medical information experience, strong knowledge of clinical trials, excellent written/verbal communication, strong organization/prioritization, oncology knowledge preferred, at least two years relevant experience, etc.
- Benefits: mention ACA-compliant supplemental package available for enrollment. Also note no PTO, no Benefits (but that's a negative). The instruction: only include Benefits section if posting actually states them. It does state "ACA-compliant supplemental package available for enrollment." That's a benefit. Also "W2 contract, no PTO, no Benefits." That's not a benefit but we could mention lack of benefits? Probably not include as benefit. We'll include the supplemental package.
- Pay: include "$65.00 - $85.00/hr".
- Schedule: "Hybrid schedule of three flexible onsite days per week." Also note location Upper Gwynedd, PA requires 3 days in office.
We must not include boilerplate like EEO, etc.
We must not repeat job title as heading.
We must not include Job ID.
We must output only HTML fragment, no /, no markdown fences.
We need to use for section headings. Use - for any list of duties/requirements/benefits, and
for prose.
We need to preserve all substantive information; do not invent or summarize away detail.
We must not emit a heading followed by filler/placeholder text. So each section must have real content.
We need to decide which sections to include.
Potential sections:
- About the role: include contract length, location, client, role title maybe? But we cannot repeat job title as heading, but we can mention it in prose.
- Responsibilities: list duties.
- Requirements: required education/experience, legal auth, W2 without sponsorship.
- Qualifications: preferred experience/skills (maybe also include some required? but we already used required in Requirements). Could combine but better separate.
- Skills: key skills list.
- Benefits: ACA-compliant supplemental package.
- Pay: pay range.
- Schedule: hybrid schedule.
We must ensure we don't duplicate content across sections unnecessarily, but we can repeat if needed? Probably avoid duplication but not strictly prohibited. However we should preserve all info; duplication okay but better to split.
Let's extract details:
About the role:
- Primary Talent Partners has a new contract opening for a Medical Affairs Specialist to join our pharmaceutical client in North Wales, PA.
- This is a 12-month contract to start with the potential for extensions.
- Hybrid position is in Upper Gwynedd, PA - requires 3 days in the office.
- Candidates must be legally authorized to work in the United States and must be able to sit on Primary Talent Partners W2 without sponsorship.
But legal auth and W2 sponsorship maybe belong to Requirements.
Let's keep About the role: location, contract length, client, role type.
Responsibilities:
- Handling of all US healthcare professional (HCP) inquiries and escalated complex global HCP inquiries.
- Generating insights and analysis.
- Medical review of promotional and non-promotional scientific materials.
- Compendia and Pathways submissions.
Requirements:
- Advanced degree (PharmD, PhD, MS or equivalent) relevant to the position.
- Some work experience in Medical Information and/or Medical/Scientific Review of promotional materials in the biotech/pharmaceutical or healthcare environment.
- Strong knowledge of clinical trial methodology, statistical concepts, and evaluation and interpretation of complex scientific literature.
- Excellent interpersonal and communication skills.
- Organizational and prioritization skills.
- Some knowledge and therapeutic area experience in Oncology.
- Candidates must be legally authorized to work in the United States.
- Must be able to sit on Primary Talent Partners W2 without sponsorship.
Qualifications (preferred):
- 2 years of medical information or medical/scientific review or relevant biotech/pharmaceutical experience.
- Deep experience working in Medical Information and/or prior biotech/pharmaceutical industry experience.
- Advanced knowledge and therapeutic area experience in Oncology.
- Strong working knowledge of Microsoft Office Suite and systems for Medical Information and Promotional Review.
- Negotiation skills for interaction with cross-functional teams.
Skills (key skills):
- Advanced scientific or clinical degree, preferably a PharmD or PhD.
- Medical review expertise (primary need).
- Medical information experience.
- Strong knowledge of clinical trials.
- Excellent written and verbal communication skills.
- Strong organization and prioritization skills.
- Oncology knowledge preferred.
- At least two years of relevant experience is required.
- Pharmaceutical, CRO, medical communications agency, fellowship, internship, and co-op experience may be considered.
But note some overlap with Requirements and Qualifications. We need to avoid duplication but we can keep distinct.
Maybe better: Requirements = required education/experience; Qualifications = preferred; Skills = key skills list (some overlapping). However the instruction: "Prefer a few substantive sections over many thin ones." So maybe we combine some.
But we must include sections only when posting has real specific content. All sections have content.
We need to decide final sections: About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule.
Let's craft each.
About the role:
Primary Talent Partners has a new contract opening for a Medical Affairs Specialist to join a pharmaceutical client in North Wales, PA. This is a 12-month contract with potential for extensions. The position is hybrid, based in Upper Gwynedd, PA, requiring three onsite days per week.
Responsibilities: - Handle all US healthcare professional (HCP) inquiries and escalated complex global HCP inquiries.
- Generate insights and analysis from inquiries.
- Perform medical review of promotional and non-promotional scientific materials.
- Prepare compendia and pathways submissions.
Requirements: - Advanced degree (PharmD, PhD, MS or equivalent) relevant to the position.
- Some work experience in Medical Information and/or Medical/Scientific Review of promotional materials in biotech/pharmaceutical or healthcare settings.
- Strong knowledge of clinical trial methodology, statistical concepts, and evaluation/interpretation of complex scientific literature.
- Excellent interpersonal and communication skills.
- Organizational and prioritization skills.
- Some knowledge and therapeutic area experience in Oncology.
- Legally authorized to work in the United States.
- Ability to sit on Primary Talent Partners W2 without sponsorship.
Qualifications (preferred): - Two years of medical information or medical/scientific review or relevant biotech/pharmaceutical experience.
- Deep experience working in Medical Information and/or prior biotech/pharmaceutical industry experience.
- Advanced knowledge and therapeutic area experience in Oncology.
- Strong working knowledge of Microsoft Office Suite and systems for Medical Information and Promotional Review.
- Negotiation skills for interaction with cross‑functional teams.
Skills: - Advanced scientific or clinical degree, preferably a PharmD or PhD.
- Medical review expertise (primary need for the role).
- Medical information experience.
- Strong knowledge of clinical trials.
- Excellent written and verbal communication skills.
- Strong organization and prioritization skills.
- Oncology knowledge preferred.
- At least two years of relevant experience required.
- Pharmaceutical, CRO, medical communications agency, fellowship, internship, or co‑op experience may be considered.
Benefits:
- for any list of duties/requirements/benefits, and
for prose. We need to preserve all substantive information; do not invent or summarize away detail. We must not emit a heading followed by filler/placeholder text. So each section must have real content. We need to decide which sections to include. Potential sections: - About the role: include contract length, location, client, role title maybe? But we cannot repeat job title as heading, but we can mention it in prose. - Responsibilities: list duties. - Requirements: required education/experience, legal auth, W2 without sponsorship. - Qualifications: preferred experience/skills (maybe also include some required? but we already used required in Requirements). Could combine but better separate. - Skills: key skills list. - Benefits: ACA-compliant supplemental package. - Pay: pay range. - Schedule: hybrid schedule. We must ensure we don't duplicate content across sections unnecessarily, but we can repeat if needed? Probably avoid duplication but not strictly prohibited. However we should preserve all info; duplication okay but better to split. Let's extract details: About the role: - Primary Talent Partners has a new contract opening for a Medical Affairs Specialist to join our pharmaceutical client in North Wales, PA. - This is a 12-month contract to start with the potential for extensions. - Hybrid position is in Upper Gwynedd, PA - requires 3 days in the office. - Candidates must be legally authorized to work in the United States and must be able to sit on Primary Talent Partners W2 without sponsorship. But legal auth and W2 sponsorship maybe belong to Requirements. Let's keep About the role: location, contract length, client, role type. Responsibilities: - Handling of all US healthcare professional (HCP) inquiries and escalated complex global HCP inquiries. - Generating insights and analysis. - Medical review of promotional and non-promotional scientific materials. - Compendia and Pathways submissions. Requirements: - Advanced degree (PharmD, PhD, MS or equivalent) relevant to the position. - Some work experience in Medical Information and/or Medical/Scientific Review of promotional materials in the biotech/pharmaceutical or healthcare environment. - Strong knowledge of clinical trial methodology, statistical concepts, and evaluation and interpretation of complex scientific literature. - Excellent interpersonal and communication skills. - Organizational and prioritization skills. - Some knowledge and therapeutic area experience in Oncology. - Candidates must be legally authorized to work in the United States. - Must be able to sit on Primary Talent Partners W2 without sponsorship. Qualifications (preferred): - 2 years of medical information or medical/scientific review or relevant biotech/pharmaceutical experience. - Deep experience working in Medical Information and/or prior biotech/pharmaceutical industry experience. - Advanced knowledge and therapeutic area experience in Oncology. - Strong working knowledge of Microsoft Office Suite and systems for Medical Information and Promotional Review. - Negotiation skills for interaction with cross-functional teams. Skills (key skills): - Advanced scientific or clinical degree, preferably a PharmD or PhD. - Medical review expertise (primary need). - Medical information experience. - Strong knowledge of clinical trials. - Excellent written and verbal communication skills. - Strong organization and prioritization skills. - Oncology knowledge preferred. - At least two years of relevant experience is required. - Pharmaceutical, CRO, medical communications agency, fellowship, internship, and co-op experience may be considered. But note some overlap with Requirements and Qualifications. We need to avoid duplication but we can keep distinct. Maybe better: Requirements = required education/experience; Qualifications = preferred; Skills = key skills list (some overlapping). However the instruction: "Prefer a few substantive sections over many thin ones." So maybe we combine some. But we must include sections only when posting has real specific content. All sections have content. We need to decide final sections: About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. Let's craft each. About the role:
Primary Talent Partners has a new contract opening for a Medical Affairs Specialist to join a pharmaceutical client in North Wales, PA. This is a 12-month contract with potential for extensions. The position is hybrid, based in Upper Gwynedd, PA, requiring three onsite days per week.
Responsibilities:- Handle all US healthcare professional (HCP) inquiries and escalated complex global HCP inquiries.
- Generate insights and analysis from inquiries.
- Perform medical review of promotional and non-promotional scientific materials.
- Prepare compendia and pathways submissions.
- Advanced degree (PharmD, PhD, MS or equivalent) relevant to the position.
- Some work experience in Medical Information and/or Medical/Scientific Review of promotional materials in biotech/pharmaceutical or healthcare settings.
- Strong knowledge of clinical trial methodology, statistical concepts, and evaluation/interpretation of complex scientific literature.
- Excellent interpersonal and communication skills.
- Organizational and prioritization skills.
- Some knowledge and therapeutic area experience in Oncology.
- Legally authorized to work in the United States.
- Ability to sit on Primary Talent Partners W2 without sponsorship.
- Two years of medical information or medical/scientific review or relevant biotech/pharmaceutical experience.
- Deep experience working in Medical Information and/or prior biotech/pharmaceutical industry experience.
- Advanced knowledge and therapeutic area experience in Oncology.
- Strong working knowledge of Microsoft Office Suite and systems for Medical Information and Promotional Review.
- Negotiation skills for interaction with cross‑functional teams.
- Advanced scientific or clinical degree, preferably a PharmD or PhD.
- Medical review expertise (primary need for the role).
- Medical information experience.
- Strong knowledge of clinical trials.
- Excellent written and verbal communication skills.
- Strong organization and prioritization skills.
- Oncology knowledge preferred.
- At least two years of relevant experience required.
- Pharmaceutical, CRO, medical communications agency, fellowship, internship, or co‑op experience may be considered.